A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10349n54



Internal ID20143773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29888682..29917019hg38UCSC Ensembl
chr6:29856459..29884796hg19UCSC Ensembl
chr6:29964438..29992775hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3828338
hg1928338
hg1828338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601342, nsv601353, nsv601313, nsv601343, nsv601291, nsv601312
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10349n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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