A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055601



Internal ID18798132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45664548..45687696hg38UCSC Ensembl
Innerchr20:44293187..44316335hg19UCSC Ensembl
Innerchr20:43726601..43749749hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3823149
hg1923149
hg1823149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584841
Samples
Known GenesWFDC10B, WFDC11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055601
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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