A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661937



Internal ID9928042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36603723..36609034hg38UCSC Ensembl
Outerchr10:36603566..36609187hg38UCSC Ensembl
Innerchr10:36892651..36897962hg19UCSC Ensembl
Outerchr10:36892494..36898115hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385622
hg195622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5571418, essv6105934
SamplesNA18621, NA18565
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661937
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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