A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15249964



Internal ID6099240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53204483..53213150hg38UCSC Ensembl
Innerchr15:53204499..53213135hg38UCSC Ensembl
Outerchr15:53204468..53213166hg38UCSC Ensembl
chr15:53496680..53505347hg19UCSC Ensembl
Innerchr15:53496696..53505332hg19UCSC Ensembl
Outerchr15:53496665..53505363hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg388668
hg198668
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636503
Supporting Variants
SamplesNA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15249964
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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