A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15249442



Internal ID4105041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52959511..52992364hg38UCSC Ensembl
Innerchr15:52959543..52992333hg38UCSC Ensembl
Outerchr15:52959480..52992396hg38UCSC Ensembl
chr15:53251708..53284561hg19UCSC Ensembl
Innerchr15:53251740..53284530hg19UCSC Ensembl
Outerchr15:53251677..53284593hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3832854
hg1932854
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636498
Supporting Variants
SamplesHG03729
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15249442
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