A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15271669



Internal ID936574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64868398..64869384hg38UCSC Ensembl
Innerchr15:64868465..64869318hg38UCSC Ensembl
Outerchr15:64868332..64869451hg38UCSC Ensembl
chr15:65160597..65161583hg19UCSC Ensembl
Innerchr15:65160664..65161517hg19UCSC Ensembl
Outerchr15:65160531..65161650hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636746
Supporting Variants
SamplesHG00559
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15271669
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