A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930368



Internal ID16224324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:202033574..202035234hg38UCSC Ensembl
Innerchr2:202898297..202899957hg19UCSC Ensembl
Innerchr2:202606542..202608202hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381661
hg191661
hg181661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584174
Supporting Variants
Samples
Known GenesFZD7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv930368
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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