A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667465



Internal ID9586884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72100674..72103369hg38UCSC Ensembl
Outerchr10:72100614..72103437hg38UCSC Ensembl
Innerchr10:73860432..73863127hg19UCSC Ensembl
Outerchr10:73860372..73863195hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382824
hg192824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5579710, essv6525988, essv5607560
SamplesNA19916, NA19197, NA19818
Known GenesASCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667465
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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