A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665040



Internal ID2898127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99057793..99060106hg38UCSC Ensembl
Outerchr10:99057636..99060259hg38UCSC Ensembl
Innerchr10:100817550..100819863hg19UCSC Ensembl
Outerchr10:100817393..100820016hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382624
hg192624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6038054
SamplesHG00708
Known GenesHPSE2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665040
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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