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nsv5471620

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,171

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
Submitted genomic75,594,050-75,596,220Question Mark
Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):74,889,875-74,892,045Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5471620Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr575,594,05075,596,220
nsv5471620RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr574,889,87574,892,045

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967131deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967131Submitted genomicNC_000005.10:g.755
94050_75596220del
GRCh38 (hg38)NC_000005.10Chr575,594,05075,596,220
nssv16967131RemappedPerfectNC_000005.9:g.7488
9875_74892045del
GRCh37.p13First PassNC_000005.9Chr574,889,87574,892,045

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)
nssv16967131<0.00126404
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