A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674862



Internal ID9594281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29798436..29954897hg38UCSC Ensembl
chr6:29766213..29922674hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38156462
hg19156462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1086e199
Supporting Variantsessv5803929, essv5835605, essv5832836, essv5407765, essv5822859, essv6109636, essv5672489, essv6185173, essv5755571
SamplesNA11830, NA19399, NA18959, NA18940, NA19087, NA18520, NA19395, NA19785, NA20807
Known GenesHCG4B, HLA-A, HLA-G, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674862
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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