A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586081



Internal ID18884362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53546616..53564213hg38UCSC Ensembl
Innerchr20:52163155..52180752hg19UCSC Ensembl
Innerchr20:51596562..51614159hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3817598
hg1917598
hg1817598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062713
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)nssv3586081
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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