A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099838



Internal ID21269320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41616096..41619257hg38UCSC Ensembl
Innerchr20:40244735..40247896hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg383162
hg193162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114777
Supporting Variants
Samplessample138
Known GenesCHD6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099838
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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