A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665204



Internal ID9931309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18927737..19089058hg38UCSC Ensembl
Innerchr10:19216666..19377987hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38161322
hg19161322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5547041
SamplesNA19240
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665204
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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