A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv800050



Internal ID15747320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89708819..89709513hg38UCSC Ensembl
Innerchr12:90102596..90103290hg19UCSC Ensembl
Innerchr12:88626727..88627421hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38695
hg19695
hg18695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559717
Supporting Variants
Samples
Known GenesLINC00936
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv800050
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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