A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15245743



Internal ID1899316
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636431
Supporting Variants
SamplesHG01784
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15245743
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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