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nsv5454311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:178,063

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 449 SVs from 50 studies. See in: genome view    
Submitted genomic75,531,063-75,709,125Question Mark
Overlapping variant regions from other studies: 449 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):74,826,888-75,004,950Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5454311Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr575,531,06375,709,125
nsv5454311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr574,826,88875,004,950

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17735387duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17735387Submitted genomicNC_000005.10:g.755
31063_75709125dup
GRCh38 (hg38)NC_000005.10Chr575,531,06375,709,125
nssv17735387RemappedPerfectNC_000005.9:g.7482
6888_75004950dup
GRCh37.p13First PassNC_000005.9Chr574,826,88875,004,950

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)
nssv17735387<0.00116404
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