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nsv4058070

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 43 SVs from 13 studies. See in: genome view    
Remapped(Score: Good):149,779,444-149,821,445Question Mark
Overlapping variant regions from other studies: 70 SVs from 15 studies. See in: genome view    
Submitted genomic149,751,000-149,793,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4058070RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1149,779,444149,821,445
nsv4058070Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1149,751,000149,793,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15963285duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15963285RemappedGoodNC_000001.11:g.149
779444_149821445du
p
GRCh38.p12First PassNC_000001.11Chr1149,779,444149,821,445
nssv15963285Submitted genomicNC_000001.10:g.149
751000_149793000du
p
GRCh37.p13NC_000001.10Chr1149,751,000149,793,000

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)
nssv15963285<0.001421690
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