A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1105e199



Internal ID22758878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32511648..32589728hg38UCSC Ensembl
chr6:32479425..32557505hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3878081
hg1978081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664021, esv2669071, esv2664778, esv2664867, esv2670941, esv2659240, esv2676073
SamplesHG01259, NA19908, HG01345, NA18566, HG01497, NA18536, HG00240, HG00372
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1105e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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