A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6391878



Internal ID9369281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29883740..29938567hg38UCSC Ensembl
chr6:29851517..29906344hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854828
hg1954828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657754
Supporting Variants
SamplesHG00121
Known GenesHCG4B, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6391878
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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