A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5707053



Internal ID9447006
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 Flag1
Merged StatusS
Merged Variantsesv2665936
Supporting Variants
SamplesNA18867
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5707053
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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