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nsv5475971

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,454

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 268 SVs from 39 studies. See in: genome view    
Submitted genomic127,704,200-127,717,653Question Mark
Overlapping variant regions from other studies: 269 SVs from 39 studies. See in: genome view    
Remapped(Score: Good):128,716,445-128,729,899Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5475971Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8127,704,200127,717,653
nsv5475971RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8128,716,445128,729,899

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17016419deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17016419Submitted genomicNC_000008.11:g.127
704200_127717653de
l
GRCh38 (hg38)NC_000008.11Chr8127,704,200127,717,653
nssv17016419RemappedGoodNC_000008.10:g.128
716445_128729899de
l
GRCh37.p13First PassNC_000008.10Chr8128,716,445128,729,899

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17016419<0.00126404
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