A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583903



Internal ID18882184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192516979..192557140hg38UCSC Ensembl
Innerchr2:193381705..193421866hg19UCSC Ensembl
Innerchr2:193089950..193130111hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3840162
hg1940162
hg1840162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010559
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)nssv3583903
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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