A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675070



Internal ID9941175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21396362..21398163hg38UCSC Ensembl
Outerchr10:21396205..21398316hg38UCSC Ensembl
Innerchr10:21685291..21687092hg19UCSC Ensembl
Outerchr10:21685134..21687245hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382112
hg192112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv124e199
Supporting Variantsessv5868423, essv5549424
SamplesHG00342, HG00310
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675070
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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