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nsv4987341

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,796

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 21 studies. See in: genome view    
Submitted genomic75,411,660-75,413,461Question Mark
Overlapping variant regions from other studies: 88 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):75,122,704-75,124,505Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4987341Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1175,411,663 (-3, +35)75,413,458 (-35, +3)
nsv4987341RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1175,122,707 (-3, +35)75,124,502 (-35, +3)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16528181deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16528181Submitted genomicNC_000011.10:g.(75
411660_75411698)_(
75413423_75413461)
del
GRCh38 (hg38)NC_000011.10Chr1175,411,663 (-3, +35)75,413,458 (-35, +3)
nssv16528181RemappedPerfectNC_000011.9:g.(751
22704_75122742)_(7
5124467_75124505)d
el
GRCh37.p13First PassNC_000011.9Chr1175,122,707 (-3, +35)75,124,502 (-35, +3)

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)
nssv16528181<0.001129246
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