A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686934



Internal ID15076900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62682654..62710192hg38UCSC Ensembl
Innerchr3:62668329..62695867hg19UCSC Ensembl
Innerchr3:62643369..62670907hg18UCSC Ensembl
Innerchr3:62643369..62670907hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3827539
hg1927539
hg1827539
hg1727539
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)nssv686934
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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