A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693695



Internal ID15083661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1322368..1325162hg38UCSC Ensembl
Innerchr3:1364052..1366846hg19UCSC Ensembl
Innerchr3:1339052..1341846hg18UCSC Ensembl
Innerchr3:1339052..1341846hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg382795
hg192795
hg182795
hg172795
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)nssv693695
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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