A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622462



Internal ID7009321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15982036..16017619hg38UCSC Ensembl
Innerchr10:15982036..16017619hg38UCSC Ensembl
Outerchr10:15981536..16018119hg38UCSC Ensembl
chr10:16024035..16059618hg19UCSC Ensembl
Innerchr10:16024035..16059618hg19UCSC Ensembl
Outerchr10:16023535..16060118hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3835584
hg1935584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13705891
SamplesHG02837
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622462
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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