A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15306807



Internal ID5700543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81677358..81793304hg38UCSC Ensembl
Innerchr15:81677858..81792804hg38UCSC Ensembl
Outerchr15:81676358..81794304hg38UCSC Ensembl
chr15:81969699..82085645hg19UCSC Ensembl
Innerchr15:81970199..82085145hg19UCSC Ensembl
Outerchr15:81968699..82086645hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38115947
hg19115947
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637041
Supporting Variants
SamplesNA19089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15306807
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