A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665936



Internal ID9932041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42888866..42892182hg38UCSC Ensembl
Outerchr10:42888832..42892217hg38UCSC Ensembl
Innerchr10:43384314..43387630hg19UCSC Ensembl
Outerchr10:43384280..43387665hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383386
hg193386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv134e199
Supporting Variantsessv5707053
SamplesNA18867
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665936
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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