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nsv5457146

  • 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: 153 SVs from 28 studies. See in: genome view    
Submitted genomic81,443,973-81,445,937Question Mark
Overlapping variant regions from other studies: 153 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):82,365,127-82,367,091Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457146Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr481,443,97381,445,937
nsv5457146RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr482,365,12782,367,091

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952573deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952573Submitted genomicNC_000004.12:g.814
43973_81445937del
GRCh38 (hg38)NC_000004.12Chr481,443,97381,445,937
nssv16952573RemappedPerfectNC_000004.11:g.823
65127_82367091del
GRCh37.p13First PassNC_000004.11Chr482,365,12782,367,091

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)
nssv16952573<0.00116404
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