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nsv6147313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,384

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 32 studies. See in: genome view    
Submitted genomic123,714,582-123,722,965Question Mark
Overlapping variant regions from other studies: 135 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):124,635,737-124,644,120Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4123,714,582123,722,965
nsv6147313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4124,635,737124,644,120

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16954637mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16954637Submitted genomicNC_000004.12:g.123
714582_123722965de
l
GRCh38 (hg38)NC_000004.12Chr4123,714,582123,722,965
nssv16954637RemappedPerfectNC_000004.11:g.124
635737_124644120de
l
GRCh37.p13First PassNC_000004.11Chr4124,635,737124,644,120

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)
nssv16954637<0.00136404
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