A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636892



Internal ID7023686
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292628, essv15292627
SamplesHG01173, HG01679
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636892
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer