A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677706



Internal ID9943811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71939533..71946203hg38UCSC Ensembl
chr10:73699291..73705961hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386671
hg196671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6252747, essv6036734
SamplesHG00277, HG00182
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677706
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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