A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699659



Internal ID15436311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:10522696..10545656hg38UCSC Ensembl
Innerchr12:10675295..10698255hg19UCSC Ensembl
Innerchr12:10566562..10589522hg18UCSC Ensembl
Innerchr12:10566562..10589522hg17UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3822961
hg1922961
hg1822961
hg1722961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523828
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699659
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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