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nsv1154579

  • Variant Calls:24
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,285

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 166 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):45,574,604-45,584,888Question Mark
Overlapping variant regions from other studies: 166 SVs from 54 studies. See in: genome view    
Submitted genomic46,070,052-46,080,336Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv1154579RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nsv1154579Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv4004713deletionSNP arraySNP genotyping analysis1
nssv4004714deletionSNP arraySNP genotyping analysis0
nssv4004715deletionSNP arraySNP genotyping analysis1
nssv4004716deletionSNP arraySNP genotyping analysis1
nssv4004717deletionSNP arraySNP genotyping analysis1
nssv4004718deletionSNP arraySNP genotyping analysis1
nssv4004719deletionSNP arraySNP genotyping analysis1
nssv4004720deletionSNP arraySNP genotyping analysis0
nssv4004721deletionSNP arraySNP genotyping analysis1
nssv4004722deletionSNP arraySNP genotyping analysis1
nssv4004723deletionSNP arraySNP genotyping analysis1
nssv4004724deletionSNP arraySNP genotyping analysis1
nssv4004725deletionSNP arraySNP genotyping analysis1
nssv4004726deletionSNP arraySNP genotyping analysis1
nssv4004727deletionSNP arraySNP genotyping analysis1
nssv4004728deletionSNP arraySNP genotyping analysis1
nssv4004729deletionSNP arraySNP genotyping analysis1
nssv4004730deletionSNP arraySNP genotyping analysis1
nssv4004731deletionSNP arraySNP genotyping analysis1
nssv4004732deletionSNP arraySNP genotyping analysis1
nssv4004733deletionSNP arraySNP genotyping analysis1
nssv4004734deletionSNP arraySNP genotyping analysis1
nssv4004735deletionSNP arraySNP genotyping analysis1
nssv4004736duplicationSNP arraySNP genotyping analysis3

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv4004713RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004714RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004715RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004716RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004717RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004718RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004719RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004720RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004721RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004722RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004723RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004724RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004725RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004726RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004727RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004728RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004729RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004730RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004731RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004732RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004733RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004734RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004735RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
del
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004736RemappedPerfectNC_000010.11:g.(45
574604_45577424)_(
45580787_45584888)
dup
GRCh38.p12First PassNC_000010.11Chr1045,574,60445,577,42445,580,78745,584,888
nssv4004713Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004714Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004715Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004716Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004717Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004718Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004719Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004720Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004721Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004722Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004723Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004724Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004725Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004726Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004727Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004728Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004729Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004730Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004731Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004732Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004733Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004734Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004735Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
del
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336
nssv4004736Submitted genomicNC_000010.10:g.(46
070052_46072872)_(
46076235_46080336)
dup
GRCh37 (hg19)NC_000010.10Chr1046,070,05246,072,87246,076,23546,080,336

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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