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nsv4992088

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 13 studies. See in: genome view    
Submitted genomic66,488,096-66,488,175Question Mark
Overlapping variant regions from other studies: 97 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):66,780,434-66,780,513Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4992088Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1566,488,09666,488,175
nsv4992088RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1566,780,43466,780,513

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16550883deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16550883Submitted genomicNC_000015.10:g.664
88096_66488175del
GRCh38 (hg38)NC_000015.10Chr1566,488,09666,488,175
nssv16550883RemappedPerfectNC_000015.9:g.6678
0434_66780513del
GRCh37.p13First PassNC_000015.9Chr1566,780,43466,780,513

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)
nssv16550883<0.001129246
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