A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668329



Internal ID9587748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158802946..158803576hg38UCSC Ensembl
Outerchr6:158802909..158803626hg38UCSC Ensembl
Innerchr6:159223978..159224608hg19UCSC Ensembl
Outerchr6:159223941..159224658hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1164e199
Supporting Variantsessv5541415
SamplesNA19380
Known GenesEZR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668329
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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