A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579008



Internal ID18877289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21600126..21634335hg38UCSC Ensembl
Innerchr2:21822998..21857207hg19UCSC Ensembl
Innerchr2:21676503..21710712hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3834210
hg1934210
hg1834210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011732
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)nssv3579008
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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