A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636100



Internal ID7022896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34073847..34078379hg38UCSC Ensembl
Innerchr15:34073847..34078379hg38UCSC Ensembl
Outerchr15:34073347..34078879hg38UCSC Ensembl
chr15:34366048..34370580hg19UCSC Ensembl
Innerchr15:34366048..34370580hg19UCSC Ensembl
Outerchr15:34365548..34371080hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384533
hg194533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15210424
SamplesHG01348
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636100
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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