A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661407



Internal ID9580826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74292681..74293597hg38UCSC Ensembl
chr10:76052439..76053355hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6589638, essv6251237
SamplesHG01051, HG00179
Known GenesADK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661407
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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