A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668265



Internal ID15404917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30239766..30256542hg38UCSC Ensembl
Innerchr12:30392699..30409475hg19UCSC Ensembl
Innerchr12:30283966..30300742hg18UCSC Ensembl
Innerchr12:30283966..30300742hg17UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3816777
hg1916777
hg1816777
hg1716777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516421
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668265
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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