A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15186188



Internal ID4569552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24871805..24873519hg38UCSC Ensembl
Innerchr15:24871805..24873519hg38UCSC Ensembl
Outerchr15:24871366..24874028hg38UCSC Ensembl
chr15:25116952..25118666hg19UCSC Ensembl
Innerchr15:25116952..25118666hg19UCSC Ensembl
Outerchr15:25116513..25119175hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381715
hg191715
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635912
Supporting Variants
SamplesHG04075
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15186188
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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