A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662373



Internal ID9928478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132758242..132759326hg38UCSC Ensembl
Outerchr6:132758205..132759376hg38UCSC Ensembl
Innerchr6:133079381..133080465hg19UCSC Ensembl
Outerchr6:133079344..133080515hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6258329
SamplesHG00422
Known GenesVNN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662373
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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