A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583898



Internal ID18882179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:192320619..192415588hg38UCSC Ensembl
Innerchr2:193185345..193280314hg19UCSC Ensembl
Innerchr2:192893590..192988559hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3894970
hg1994970
hg1894970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008917
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)nssv3583898
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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