A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10372n54



Internal ID22778267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31269283..31270746hg38UCSC Ensembl
chr6:31237060..31238523hg19UCSC Ensembl
chr6:31345039..31346502hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg381464
hg191464
hg181464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601499, nsv601494
Samples
Known GenesHLA-C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10372n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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