A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696254



Internal ID15086220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39296450..39356217hg38UCSC Ensembl
Innerchr3:39337941..39397708hg19UCSC Ensembl
Innerchr3:39312945..39372712hg18UCSC Ensembl
Innerchr3:39312945..39372712hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3859768
hg1959768
hg1859768
hg1759768
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518801
Supporting Variants
Samples
Known GenesCCR8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696254
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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