A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658429



Internal ID9924534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20722367..20724569hg38UCSC Ensembl
Outerchr10:20722319..20724619hg38UCSC Ensembl
Innerchr10:21011296..21013498hg19UCSC Ensembl
Outerchr10:21011248..21013548hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6486521, essv5519545, essv5956008
SamplesHG01188, HG01168, HG00152
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658429
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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