A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672917



Internal ID9939022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102094207..102101766hg38UCSC Ensembl
chr10:103853964..103861523hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg387560
hg197560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6307297, essv6376123
SamplesHG01461, NA20765
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672917
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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