A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660938



Internal ID15050904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1322368..1325520hg38UCSC Ensembl
Innerchr3:1364052..1367204hg19UCSC Ensembl
Innerchr3:1339052..1342204hg18UCSC Ensembl
Innerchr3:1339052..1342204hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383153
hg193153
hg183153
hg173153
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517343
Supporting Variants
Samples
Known GenesCNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660938
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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