A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10348n54



Internal ID22778243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29886178..29933791hg38UCSC Ensembl
chr6:29853955..29901568hg19UCSC Ensembl
chr6:29961934..30009547hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3847614
hg1947614
hg1847614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601273, nsv601280, nsv601287, nsv601345, nsv601305, nsv601279, nsv601355, nsv601328, nsv601323, nsv601281, nsv601354, nsv601324, nsv601295, nsv601290, nsv601286, nsv601282, nsv601276, nsv601335, nsv601293, nsv601320, nsv601333, nsv601270, nsv601275, nsv601288, nsv601363, nsv601289, nsv601347, nsv601364, nsv601292, nsv601327, nsv601346, nsv601362, nsv601274, nsv601358, nsv601321, nsv601352, nsv601351, nsv601379, nsv601356, nsv601306, nsv601294, nsv601297, nsv601325, nsv601326, nsv601285, nsv601283, nsv601296, nsv601322
Samples
Known GenesHCG4B, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10348n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss93
Observed Complex0
Frequencyn/a


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