A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10521n54



Internal ID22778416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32504326..32540452hg38UCSC Ensembl
chr6:32472103..32508229hg19UCSC Ensembl
chr6:32580081..32616207hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3836127
hg1936127
hg1836127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602349, nsv602384, nsv602371
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10521n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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