A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15333421



Internal ID1859557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97362688..97372195hg38UCSC Ensembl
Innerchr15:97362688..97372195hg38UCSC Ensembl
Outerchr15:97362188..97372695hg38UCSC Ensembl
chr15:97905918..97915425hg19UCSC Ensembl
Innerchr15:97905918..97915425hg19UCSC Ensembl
Outerchr15:97905418..97915925hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg389508
hg199508
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637376
Supporting Variants
SamplesHG01761
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15333421
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