A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692876



Internal ID15082842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62679605..62708646hg38UCSC Ensembl
Innerchr3:62665280..62694321hg19UCSC Ensembl
Innerchr3:62640320..62669361hg18UCSC Ensembl
Innerchr3:62640320..62669361hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3829042
hg1929042
hg1829042
hg1729042
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516380
Supporting Variants
Samples
Known GenesCADPS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692876
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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