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nsv5465927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,965

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Submitted genomic70,902,293-70,904,257Question Mark
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):71,768,010-71,769,974Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr470,902,29370,904,257
nsv5465927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr471,768,01071,769,974

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16950655deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16950655Submitted genomicNC_000004.12:g.709
02293_70904257del
GRCh38 (hg38)NC_000004.12Chr470,902,29370,904,257
nssv16950655RemappedPerfectNC_000004.11:g.717
68010_71769974del
GRCh37.p13First PassNC_000004.11Chr471,768,01071,769,974

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)
nssv16950655<0.00116404
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