A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930367



Internal ID15877637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:202033574..202034725hg38UCSC Ensembl
Innerchr2:202898297..202899448hg19UCSC Ensembl
Innerchr2:202606542..202607693hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381152
hg191152
hg181152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584173
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)nssv930367
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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