A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637395



Internal ID7024187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98113406..98127796hg38UCSC Ensembl
Innerchr15:98113417..98127786hg38UCSC Ensembl
Outerchr15:98113396..98127807hg38UCSC Ensembl
chr15:98656635..98671025hg19UCSC Ensembl
Innerchr15:98656646..98671015hg19UCSC Ensembl
Outerchr15:98656625..98671036hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3814391
hg1914391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15334481
SamplesHG01600
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637395
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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