A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15316904



Internal ID5583658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88350512..88353552hg38UCSC Ensembl
Innerchr15:88350524..88353540hg38UCSC Ensembl
Outerchr15:88350500..88353564hg38UCSC Ensembl
chr15:88893743..88896783hg19UCSC Ensembl
Innerchr15:88893755..88896771hg19UCSC Ensembl
Outerchr15:88893731..88896795hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383041
hg193041
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637169
Supporting Variants
SamplesNA19025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15316904
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