A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15185099



Internal ID537578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24870548..24872350hg38UCSC Ensembl
Innerchr15:24870550..24872349hg38UCSC Ensembl
Outerchr15:24870547..24872352hg38UCSC Ensembl
chr15:25115695..25117497hg19UCSC Ensembl
Innerchr15:25115697..25117496hg19UCSC Ensembl
Outerchr15:25115694..25117499hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381803
hg191803
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635911
Supporting Variants
SamplesHG00234
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15185099
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