A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581697



Internal ID18879978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52058830..52131118hg38UCSC Ensembl
Innerchr2:52285968..52358256hg19UCSC Ensembl
Innerchr2:52139472..52211760hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3872289
hg1972289
hg1872289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000249
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)nssv3581697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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