A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15248860



Internal ID5486894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52083634..52086168hg38UCSC Ensembl
Innerchr15:52083634..52086168hg38UCSC Ensembl
Outerchr15:52083309..52086449hg38UCSC Ensembl
chr15:52375831..52378365hg19UCSC Ensembl
Innerchr15:52375831..52378365hg19UCSC Ensembl
Outerchr15:52375506..52378646hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636480
Supporting Variants
SamplesNA18980
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15248860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer