A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587559



Internal ID18539154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54035424..54046023hg38UCSC Ensembl
Innerchr20:52651963..52662562hg19UCSC Ensembl
Innerchr20:52085370..52095969hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810600
hg1910600
hg1810600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065957
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)nssv3587559
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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