A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622473



Internal ID7009332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16529310..16530762hg38UCSC Ensembl
Innerchr10:16529327..16530746hg38UCSC Ensembl
Outerchr10:16529294..16530779hg38UCSC Ensembl
chr10:16571309..16572761hg19UCSC Ensembl
Innerchr10:16571326..16572745hg19UCSC Ensembl
Outerchr10:16571293..16572778hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381453
hg191453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13706304
SamplesHG03814
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622473
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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