A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10572n54



Internal ID22778467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32581804..32659937hg38UCSC Ensembl
chr6:32549581..32627714hg19UCSC Ensembl
chr6:32657559..32735692hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3878134
hg1978134
hg1878134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602680, nsv602658, nsv602648, nsv602691, nsv602630, nsv602663, nsv602687, nsv602664, nsv602672, nsv602667, nsv602628
SamplesHGDP00066
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10572n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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