A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656916



Internal ID9576335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15627760..15632203hg38UCSC Ensembl
Outerchr10:15627723..15632253hg38UCSC Ensembl
Innerchr10:15669759..15674202hg19UCSC Ensembl
Outerchr10:15669722..15674252hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384531
hg194531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6192850
SamplesNA18522
Known GenesITGA8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656916
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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