A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602824



Internal ID16043547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33087084..33093172hg38UCSC Ensembl
Innerchr6:33054861..33060949hg19UCSC Ensembl
Innerchr6:33162839..33168927hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386089
hg196089
hg186089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154295
SamplesHGDP01290
Known GenesHLA-DPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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