A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586076



Internal ID18884357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52207330..52243776hg38UCSC Ensembl
Innerchr20:50823869..50860315hg19UCSC Ensembl
Innerchr20:50257276..50293722hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3836447
hg1936447
hg1836447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061624
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)nssv3586076
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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