A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15292628



Internal ID1803060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73724969..73734005hg38UCSC Ensembl
Innerchr15:73724969..73734005hg38UCSC Ensembl
Outerchr15:73724654..73734247hg38UCSC Ensembl
chr15:74017310..74026346hg19UCSC Ensembl
Innerchr15:74017310..74026346hg19UCSC Ensembl
Outerchr15:74016995..74026588hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg389037
hg199037
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636892
Supporting Variants
SamplesHG01679
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15292628
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