U.S. flag

An official website of the United States government

nsv932753

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,223,611

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 4889 SVs from 116 studies. See in: genome view    
Remapped(Score: Perfect):110,226,128-112,449,738Question Mark
Overlapping variant regions from other studies: 4886 SVs from 116 studies. See in: genome view    
Submitted genomic110,983,705-113,207,315Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv932753RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2110,226,128110,634,615112,347,094112,449,738
nsv932753Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr2110,983,705111,392,192113,104,671113,207,315

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1611181duplication1873Oligo aCGHProbe signal intensity
nssv1611492deletion1782Oligo aCGHProbe signal intensity
nssv1612706duplication1721Oligo aCGHProbe signal intensity
nssv1611032deletion688Oligo aCGHProbe signal intensitynssv1611809
nssv1611174deletion654Oligo aCGHProbe signal intensitynssv1612030
nssv1611574deletion463Oligo aCGHProbe signal intensity
nssv1611994deletion491Oligo aCGHProbe signal intensity
nssv1612333deletion581Oligo aCGHProbe signal intensity
nssv1610625duplication1672Oligo aCGHProbe signal intensitynssv1611206
nssv1611390deletion1430Oligo aCGHProbe signal intensity
nssv1612142deletion1592Oligo aCGHProbe signal intensity
nssv1612461deletion1801Oligo aCGHProbe signal intensity
nssv1612548deletion1504Oligo aCGHProbe signal intensity
nssv1612589deletion806Oligo aCGHProbe signal intensity
nssv1612124duplication49Oligo aCGHProbe signal intensity
nssv1612544duplication456Oligo aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1611181RemappedPerfectNC_000002.12:g.(11
0226126_110649261)
_(112271200_112297
376)dup
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,649,261112,271,200112,297,376
nssv1611492RemappedPerfectNC_000002.12:g.(11
0226126_110649261)
_(112345017_112452
833)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,649,261112,345,017112,452,833
nssv1612706RemappedPerfectNC_000002.12:g.(11
0226126_110649261)
_(112345017_112452
833)dup
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,649,261112,345,017112,452,833
nssv1611032RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112431389_112431
389)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,431,389112,431,389
nssv1611174RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112431389_112431
389)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,431,389112,431,389
nssv1611574RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112431389_112431
389)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,431,389112,431,389
nssv1611994RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112431389_112431
389)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,431,389112,431,389
nssv1612333RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112431389_112431
389)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,431,389112,431,389
nssv1610625RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112452833_112452
833)dup
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,452,833112,452,833
nssv1611390RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112452833_112452
833)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,452,833112,452,833
nssv1612142RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112452833_112452
833)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,452,833112,452,833
nssv1612461RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112452833_112452
833)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,452,833112,452,833
nssv1612548RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112452833_112452
833)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,452,833112,452,833
nssv1612589RemappedPassNC_000002.12:g.(11
0226126_110226126)
_(112452833_112452
833)del
GRCh38.p12First PassNC_000002.12Chr2110,226,126110,226,126112,452,833112,452,833
nssv1612124RemappedPerfectNC_000002.12:g.(11
0649320_110649320)
_(112452833_112452
833)dup
GRCh38.p12First PassNC_000002.12Chr2110,649,320110,649,320112,452,833112,452,833
nssv1612544RemappedPerfectNC_000002.12:g.(11
0703827_110721793)
_(112271200_112297
376)dup
GRCh38.p12First PassNC_000002.12Chr2110,703,827110,721,793112,271,200112,297,376
nssv1611032RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113188966_113188
966)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,188,966113,188,966
nssv1611174RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113188966_113188
966)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,188,966113,188,966
nssv1611574RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113188966_113188
966)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,188,966113,188,966
nssv1611994RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113188966_113188
966)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,188,966113,188,966
nssv1612333RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113188966_113188
966)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,188,966113,188,966
nssv1610625RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113210410_113210
410)dup
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,210,410113,210,410
nssv1611390RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113210410_113210
410)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,210,410113,210,410
nssv1612142RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113210410_113210
410)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,210,410113,210,410
nssv1612461RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113210410_113210
410)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,210,410113,210,410
nssv1612548RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113210410_113210
410)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,210,410113,210,410
nssv1612589RemappedPassNC_000002.11:g.(11
0983703_110983703)
_(113210410_113210
410)del
GRCh37.p13First PassNC_000002.11Chr2110,983,703110,983,703113,210,410113,210,410
nssv1612124RemappedPerfectNC_000002.11:g.(11
1406897_111406897)
_(113210410_113210
410)dup
GRCh37.p13First PassNC_000002.11Chr2111,406,897111,406,897113,210,410113,210,410
nssv1612544RemappedPerfectNC_000002.11:g.(11
1461404_111479370)
_(113028777_113054
953)dup
GRCh37.p13First PassNC_000002.11Chr2111,461,404111,479,370113,028,777113,054,953
nssv1611181Submitted genomicNC_000002.11:g.(11
0983703_111406838)
_(113028777_113054
953)dup
GRCh37 (hg19)NC_000002.11Chr2110,983,703111,406,838113,028,777113,054,953
nssv1611492Submitted genomicNC_000002.11:g.(11
0983703_111406838)
_(113102594_113210
410)del
GRCh37 (hg19)NC_000002.11Chr2110,983,703111,406,838113,102,594113,210,410
nssv1612706Submitted genomicNC_000002.11:g.(11
0983703_111406838)
_(113102594_113210
410)dup
GRCh37 (hg19)NC_000002.11Chr2110,983,703111,406,838113,102,594113,210,410
nssv1610625Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112926
881)dup
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,926,881
nssv1611032Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112905
437)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,905,437
nssv1611174Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112905
437)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,905,437
nssv1611390Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112926
881)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,926,881
nssv1611574Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112905
437)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,905,437
nssv1611994Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112905
437)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,905,437
nssv1612142Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112926
881)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,926,881
nssv1612333Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112905
437)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,905,437
nssv1612461Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112926
881)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,926,881
nssv1612548Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112926
881)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,926,881
nssv1612589Submitted genomicNC_000002.10:g.(11
0340992_111123310)
_(112819065_112926
881)del
NCBI36 (hg18)NC_000002.10Chr2110,340,992111,123,310112,819,065112,926,881
nssv1612124Submitted genomicNC_000002.10:g.(11
1123369_111131610)
_(112819065_112926
881)dup
NCBI36 (hg18)NC_000002.10Chr2111,123,369111,131,610112,819,065112,926,881
nssv1612544Submitted genomicNC_000002.10:g.(11
1177875_111195841)
_(112745248_112771
424)dup
NCBI36 (hg18)NC_000002.10Chr2111,177,875111,195,841112,745,248112,771,424

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

Support Center