A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623749



Internal ID7010605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69578285..69588420hg38UCSC Ensembl
Innerchr10:69578285..69588420hg38UCSC Ensembl
Outerchr10:69577785..69588920hg38UCSC Ensembl
chr10:71338041..71348176hg19UCSC Ensembl
Innerchr10:71338041..71348176hg19UCSC Ensembl
Outerchr10:71337541..71348676hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3810136
hg1910136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13856325
SamplesNA19795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623749
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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