A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636599



Internal ID7023393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56855215..56856654hg38UCSC Ensembl
Innerchr15:56855253..56856616hg38UCSC Ensembl
Outerchr15:56855177..56856692hg38UCSC Ensembl
chr15:57147413..57148852hg19UCSC Ensembl
Innerchr15:57147451..57148814hg19UCSC Ensembl
Outerchr15:57147375..57148890hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15259115
SamplesNA12778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636599
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