A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15317062



Internal ID5226138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89040357..89053050hg38UCSC Ensembl
Innerchr15:89040412..89052995hg38UCSC Ensembl
Outerchr15:89040302..89053105hg38UCSC Ensembl
chr15:89583588..89596281hg19UCSC Ensembl
Innerchr15:89583643..89596226hg19UCSC Ensembl
Outerchr15:89583533..89596336hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812694
hg1912694
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637185
Supporting Variants
SamplesNA18624
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15317062
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