A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113164



Internal ID21296430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135256013..135260447hg38UCSC Ensembl
Innerchr6:135577151..135581585hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg384435
hg194435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086333
Samplessample122
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113164
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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