A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10351n54



Internal ID22778246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29890188..29908663hg38UCSC Ensembl
chr6:29857965..29876440hg19UCSC Ensembl
chr6:29965944..29984419hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3818476
hg1918476
hg1818476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601310, nsv601349, nsv601341, nsv601303, nsv601311, nsv601309, nsv601308
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10351n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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