A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10553n54



Internal ID22778448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32553420..32557458hg38UCSC Ensembl
chr6:32521197..32525235hg19UCSC Ensembl
chr6:32629175..32633213hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384039
hg194039
hg184039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602515, nsv602520
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10553n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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