A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15186835



Internal ID1384110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25087750..25088893hg38UCSC Ensembl
Innerchr15:25087750..25088893hg38UCSC Ensembl
Outerchr15:25087357..25089339hg38UCSC Ensembl
chr15:25332897..25334040hg19UCSC Ensembl
Innerchr15:25332897..25334040hg19UCSC Ensembl
Outerchr15:25332504..25334486hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635918
Supporting Variants
SamplesHG01253
Known GenesSNORD116-20, SNORD116-21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15186835
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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