A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15319456



Internal ID2207027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91811758..91812744hg38UCSC Ensembl
Innerchr15:91811759..91812744hg38UCSC Ensembl
Outerchr15:91811758..91812745hg38UCSC Ensembl
chr15:92354988..92355974hg19UCSC Ensembl
Innerchr15:92354989..92355974hg19UCSC Ensembl
Outerchr15:92354988..92355975hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637248
Supporting Variants
SamplesHG01986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15319456
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