A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665189



Internal ID9584608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96637318..96642869hg38UCSC Ensembl
Outerchr10:96637281..96642919hg38UCSC Ensembl
Innerchr10:98397075..98402626hg19UCSC Ensembl
Outerchr10:98397038..98402676hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg385639
hg195639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6371252
SamplesNA19700
Known GenesPIK3AP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665189
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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