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nsv4279387

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:610,524

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 613 SVs from 21 studies. See in: genome view    
Remapped(Score: Good):20,957,148-21,567,671Question Mark
Overlapping variant regions from other studies: 613 SVs from 21 studies. See in: genome view    
Submitted genomic22,329,465-22,939,992Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4279387RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000021.9Chr2120,957,14821,567,671
nsv4279387Submitted genomicGRCh37.p13Primary AssemblyNC_000021.8Chr2122,329,46522,939,992

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15965634duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15965634RemappedGoodNC_000021.9:g.2095
7148_21567671dup
GRCh38.p12First PassNC_000021.9Chr2120,957,14821,567,671
nssv15965634Submitted genomicNC_000021.8:g.2232
9465_22939992dup
GRCh37.p13NC_000021.8Chr2122,329,46522,939,992

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)
nssv159656344.6e-005121694
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