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nsv5421861

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117,520

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 472 SVs from 58 studies. See in: genome view    
Submitted genomic46,036,519-46,154,038Question Mark
Overlapping variant regions from other studies: 472 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):46,502,191-46,619,710Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5421861Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,036,51946,154,038
nsv5421861RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr146,502,19146,619,710

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16904903duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16904903Submitted genomicNC_000001.11:g.460
36519_46154038dup
GRCh38 (hg38)NC_000001.11Chr146,036,51946,154,038
nssv16904903RemappedPerfectNC_000001.10:g.465
02191_46619710dup
GRCh37.p13First PassNC_000001.10Chr146,502,19146,619,710

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)
nssv16904903<0.00116404
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