A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584782



Internal ID18883063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41745171..41801147hg38UCSC Ensembl
Innerchr20:40373810..40429787hg19UCSC Ensembl
Innerchr20:39807224..39863201hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3855977
hg1955978
hg1855978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061830
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)nssv3584782
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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