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nsv4974004

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:158,621

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 456 SVs from 58 studies. See in: genome view    
Submitted genomic103,392,774-103,551,394Question Mark
Overlapping variant regions from other studies: 456 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):105,152,531-105,311,151Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4974004Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10103,392,774103,551,394
nsv4974004RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10105,152,531105,311,151

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16532522duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16532522Submitted genomicNC_000010.11:g.103
392774_103551394du
p
GRCh38 (hg38)NC_000010.11Chr10103,392,774103,551,394
nssv16532522RemappedPerfectNC_000010.10:g.105
152531_105311151du
p
GRCh37.p13First PassNC_000010.10Chr10105,152,531105,311,151

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)
nssv16532522<0.001129246
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