A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586101



Internal ID18537696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031269..54042022hg38UCSC Ensembl
Innerchr20:52647808..52658561hg19UCSC Ensembl
Innerchr20:52081215..52091968hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810754
hg1910754
hg1810754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064515
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)nssv3586101
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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