A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2936249



Internal ID15776585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32556461..32604823hg38UCSC Ensembl
Innerchr6:32524238..32572600hg19UCSC Ensembl
Innerchr6:32632216..32680578hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3848363
hg1948363
hg1848363
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515036
Supporting Variants
SamplesNA21310
Known GenesHLA-DRB1, HLA-DRB6
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2936249
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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