A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675622



Internal ID9941727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149355629..149364578hg38UCSC Ensembl
chr6:149676765..149685714hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg388950
hg198950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6555890
SamplesNA19093
Known GenesTAB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675622
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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