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nsv4773279

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,942

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):43,144,337-43,148,279Question Mark
Overlapping variant regions from other studies: 130 SVs from 24 studies. See in: genome view    
Submitted genomic43,610,008-43,613,950Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4773279RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr143,144,338 (-1)43,148,279 (-1)
nsv4773279Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr143,610,009 (-1)43,613,950 (-1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16310258deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16310258RemappedPerfectNC_000001.11:g.(43
144337_?)_(4314827
8_?)del
GRCh38.p12First PassNC_000001.11Chr143,144,338 (-1)43,148,279 (-1)
nssv16310258Submitted genomicNC_000001.10:g.(43
610008_?)_(4361394
9_?)del
GRCh37 (hg19)NC_000001.10Chr143,610,009 (-1)43,613,950 (-1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16310258<0.001116834
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