A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674595



Internal ID9940700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102775713..102781157hg38UCSC Ensembl
Outerchr10:102775676..102781207hg38UCSC Ensembl
Innerchr10:104535470..104540914hg19UCSC Ensembl
Outerchr10:104535433..104540964hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385532
hg195532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5860016
SamplesNA19067
Known GenesWBP1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674595
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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