A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117626



Internal ID21300892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15156618..15181339hg38UCSC Ensembl
Innerchr11:15178164..15202885hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3824722
hg1924722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091914
Samplessample237
Known GenesINSC
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117626
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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