A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668731



Internal ID9934836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5872853..5874108hg38UCSC Ensembl
Outerchr10:5872816..5874158hg38UCSC Ensembl
Innerchr10:5914816..5916071hg19UCSC Ensembl
Outerchr10:5914779..5916121hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6154079, essv5511251, essv6237544
SamplesNA19107, NA06984, HG01183
Known GenesANKRD16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668731
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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