A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667481



Internal ID9586900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95596071..95611031hg38UCSC Ensembl
Outerchr6:95596034..95611081hg38UCSC Ensembl
Innerchr6:96043947..96058907hg19UCSC Ensembl
Outerchr6:96043910..96058957hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3815048
hg1915048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6436575
SamplesNA18536
Known GenesMANEA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667481
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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