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nsv6113464

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 170 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):84,007,573-84,007,624Question Mark
Overlapping variant regions from other studies: 171 SVs from 33 studies. See in: genome view    
Submitted genomic84,676,325-84,676,376Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6113464RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1584,007,57384,007,624
nsv6113464Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000015.9Chr1584,676,32584,676,376

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17964387alu insertionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17964387RemappedPerfectNC_000015.10:g.840
07573_84007624ins?
GRCh38.p12First PassNC_000015.10Chr1584,007,57384,007,624
nssv17964387Submitted genomicNC_000015.9:g.8467
6325_84676376ins?
GRCh37 (hg19)NC_000015.9Chr1584,676,32584,676,376

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv179643870.011696404
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