A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677025



Internal ID9596444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29883324..29938168hg38UCSC Ensembl
chr6:29851101..29905945hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854845
hg1954845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1087e199
Supporting Variantsessv6427602
SamplesHG00419
Known GenesHCG4B, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677025
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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