A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15214188



Internal ID599067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35391766..35429360hg38UCSC Ensembl
Innerchr15:35391775..35429351hg38UCSC Ensembl
Outerchr15:35391757..35429369hg38UCSC Ensembl
chr15:35683967..35721561hg19UCSC Ensembl
Innerchr15:35683976..35721552hg19UCSC Ensembl
Outerchr15:35683958..35721570hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3837595
hg1937595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636135
Supporting Variants
SamplesHG00262
Known GenesDPH6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15214188
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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