A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662630



Internal ID9928735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25893724..25905329hg38UCSC Ensembl
Outerchr6:25893687..25905379hg38UCSC Ensembl
Innerchr6:25893952..25905557hg19UCSC Ensembl
Outerchr6:25893915..25905607hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3811693
hg1911693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5565774, essv6342734
SamplesNA19066, NA19076
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662630
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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