A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15186776



Internal ID4497522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24889510..24901394hg38UCSC Ensembl
Innerchr15:24889510..24901394hg38UCSC Ensembl
Outerchr15:24889295..24901595hg38UCSC Ensembl
chr15:25134657..25146541hg19UCSC Ensembl
Innerchr15:25134657..25146541hg19UCSC Ensembl
Outerchr15:25134442..25146742hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811885
hg1911885
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635913
Supporting Variants
SamplesHG03998
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15186776
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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