A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697817



Internal ID15087783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:96984349..97000154hg38UCSC Ensembl
Innerchr12:97378127..97393932hg19UCSC Ensembl
Innerchr12:95902258..95918063hg18UCSC Ensembl
Innerchr12:95880595..95896400hg17UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3815806
hg1915806
hg1815806
hg1715806
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521154
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697817
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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