A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15346489



Internal ID6364366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99969518..100058907hg38UCSC Ensembl
chr15:100509723..100599112hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3889390
hg1989390
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637454
Supporting Variants
SamplesNA20294
Known GenesADAMTS17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15346489
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