A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113655



Internal ID21296921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65923863..65928024hg38UCSC Ensembl
Innerchr5:65219691..65223852hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg384162
hg194162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108401
Samplessample138
Known GenesERBB2IP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113655
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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