A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637376



Internal ID7024169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97362688..97372195hg38UCSC Ensembl
Innerchr15:97362688..97372195hg38UCSC Ensembl
Outerchr15:97362188..97372695hg38UCSC Ensembl
chr15:97905918..97915425hg19UCSC Ensembl
Innerchr15:97905918..97915425hg19UCSC Ensembl
Outerchr15:97905418..97915925hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg389508
hg199508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15333421, essv15333422
SamplesNA18621, HG01761
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637376
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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