A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15186778



Internal ID4748977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24913053..24915241hg38UCSC Ensembl
Innerchr15:24913104..24915190hg38UCSC Ensembl
Outerchr15:24913002..24915292hg38UCSC Ensembl
chr15:25158200..25160388hg19UCSC Ensembl
Innerchr15:25158251..25160337hg19UCSC Ensembl
Outerchr15:25158149..25160439hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382189
hg192189
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635914
Supporting Variants
SamplesNA07347
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15186778
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