A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662619



Internal ID15052585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31217456..31253875hg38UCSC Ensembl
Innerchr12:31370390..31406809hg19UCSC Ensembl
Innerchr12:31261657..31298076hg18UCSC Ensembl
Innerchr12:31261657..31298076hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3836420
hg1936420
hg1836420
hg1736420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515974
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662619
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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