A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv787558



Internal ID16081514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9466205..9563530hg38UCSC Ensembl
Innerchr12:9618801..9716126hg19UCSC Ensembl
Innerchr12:9510068..9607393hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3897326
hg1997326
hg1897326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557404
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv787558
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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