A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv803308



Internal ID15750578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:118064662..118126282hg38UCSC Ensembl
Innerchr12:118502467..118564087hg19UCSC Ensembl
Innerchr12:116986850..117048470hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3861621
hg1961621
hg1861621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560389
Supporting Variants
Samples
Known GenesVSIG10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv803308
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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