A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10347n54



Internal ID20143771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29883666..29952688hg38UCSC Ensembl
chr6:29851443..29920465hg19UCSC Ensembl
chr6:29959422..30028444hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3869023
hg1969023
hg1869023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601263, nsv601258, nsv601357, nsv601299, nsv601259, nsv601262, nsv601261, nsv601300, nsv601329, nsv601277, nsv601260, nsv601257, nsv601339, nsv601330, nsv601284, nsv601298, nsv601278
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10347n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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