A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2936832



Internal ID15713222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487461..32525353hg38UCSC Ensembl
Innerchr6:32455238..32493130hg19UCSC Ensembl
Innerchr6:32563216..32601108hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3837893
hg1937893
hg1837893
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514350
Supporting Variants
SamplesNA18966
Known GenesHLA-DRB5
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2936832
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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