A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673381



Internal ID9939486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35887501..35889133hg38UCSC Ensembl
Outerchr10:35887464..35889183hg38UCSC Ensembl
Innerchr10:36176429..36178061hg19UCSC Ensembl
Outerchr10:36176392..36178111hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381720
hg191720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6401783
SamplesHG00245
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673381
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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