A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661426



Internal ID9580845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74548248..74550331hg38UCSC Ensembl
chr10:76308006..76310089hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382084
hg192084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5704055
SamplesNA19332
Known GenesADK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661426
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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