A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658830



Internal ID9924935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78625962..78636403hg38UCSC Ensembl
Outerchr10:78625805..78636556hg38UCSC Ensembl
Innerchr10:80385719..80396160hg19UCSC Ensembl
Outerchr10:80385562..80396313hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3810752
hg1910752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6588086
SamplesNA19068
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658830
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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