A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15292637



Internal ID5294453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73818723..73875766hg38UCSC Ensembl
chr15:74111064..74168107hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3857044
hg1957044
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636896
Supporting Variants
SamplesHG01705
Known GenesTBC1D21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15292637
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