A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15339097



Internal ID6549141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99017801..99019538hg38UCSC Ensembl
Innerchr15:99017801..99019538hg38UCSC Ensembl
Outerchr15:99017643..99019680hg38UCSC Ensembl
chr15:99561030..99562767hg19UCSC Ensembl
Innerchr15:99561030..99562767hg19UCSC Ensembl
Outerchr15:99560872..99562909hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381738
hg191738
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637414
Supporting Variants
SamplesNA20752
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15339097
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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