A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6366n71



Internal ID6323986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161447161..161530735hg19UCSC Ensembl
chr5:161379739..161463313hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv883080, nsv883079
SamplesIS39944, IS34962, IS31205
Known GenesGABRG2
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6366n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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