A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579006



Internal ID18877287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21600126..21629728hg38UCSC Ensembl
Innerchr2:21822998..21852600hg19UCSC Ensembl
Innerchr2:21676503..21706105hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3829603
hg1929603
hg1829603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003122
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)nssv3579006
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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