A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622283



Internal ID7009142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8147381..8160727hg38UCSC Ensembl
Innerchr10:8147401..8160707hg38UCSC Ensembl
Outerchr10:8147361..8160747hg38UCSC Ensembl
chr10:8189344..8202690hg19UCSC Ensembl
Innerchr10:8189364..8202670hg19UCSC Ensembl
Outerchr10:8189324..8202710hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813347
hg1913347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13690314
SamplesHG03517
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622283
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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