A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669848



Internal ID9935953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21862627..21872268hg38UCSC Ensembl
chr10:22151556..22161197hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg389642
hg199642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6099850, essv6104975
SamplesNA19443, NA19198
Known GenesDNAJC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669848
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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