A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583926



Internal ID18882207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194047718..194111613hg38UCSC Ensembl
Innerchr2:194912442..194976337hg19UCSC Ensembl
Innerchr2:194620687..194684582hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3863896
hg1963896
hg1863896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009749
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583926
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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