A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676465



Internal ID15066431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31143285..31257887hg38UCSC Ensembl
Innerchr12:31296219..31410821hg19UCSC Ensembl
Innerchr12:31187486..31302088hg18UCSC Ensembl
Innerchr12:31187486..31302088hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38114603
hg19114603
hg18114603
hg17114603
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)nssv676465
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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