A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587555



Internal ID18539150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54034615..54050346hg38UCSC Ensembl
Innerchr20:52651154..52666885hg19UCSC Ensembl
Innerchr20:52084561..52100292hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3815732
hg1915732
hg1815732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055306
Supporting Variants
Samples
Known GenesBCAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3587555
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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