A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659118



Internal ID9925223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22690338..22692265hg38UCSC Ensembl
Outerchr10:22690301..22692315hg38UCSC Ensembl
Innerchr10:22979267..22981194hg19UCSC Ensembl
Outerchr10:22979230..22981244hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg382015
hg192015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6287988
SamplesNA20512
Known GenesPIP4K2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659118
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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