A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15310022



Internal ID5547386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82876135..82882267hg38UCSC Ensembl
Innerchr15:82876135..82882267hg38UCSC Ensembl
Outerchr15:82875877..82882479hg38UCSC Ensembl
chr15:83544887..83551019hg19UCSC Ensembl
Innerchr15:83544887..83551019hg19UCSC Ensembl
Outerchr15:83544629..83551231hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386133
hg196133
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637062
Supporting Variants
SamplesNA19004
Known GenesHOMER2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15310022
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