A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663703



Internal ID9929808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74711374..74712591hg38UCSC Ensembl
Outerchr10:74711340..74712626hg38UCSC Ensembl
Innerchr10:76471132..76472349hg19UCSC Ensembl
Outerchr10:76471098..76472384hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv156e199
Supporting Variantsessv5835978
SamplesNA19722
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663703
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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