A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636431



Internal ID7023225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49807516..49809039hg38UCSC Ensembl
Innerchr15:49807520..49809036hg38UCSC Ensembl
Outerchr15:49807513..49809043hg38UCSC Ensembl
chr15:50099713..50101236hg19UCSC Ensembl
Innerchr15:50099717..50101233hg19UCSC Ensembl
Outerchr15:50099710..50101240hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15245743, essv15245744
SamplesHG01784, HG03565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636431
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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