A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10598n54



Internal ID22778493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32659081..32660181hg38UCSC Ensembl
chr6:32626858..32627958hg19UCSC Ensembl
chr6:32734836..32735936hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381101
hg191101
hg181101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602777, nsv602782, nsv602781
Samples
Known GenesHLA-DQB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10598n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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