A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15226915



Internal ID879081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39466812..39479233hg38UCSC Ensembl
Innerchr15:39466825..39479221hg38UCSC Ensembl
Outerchr15:39466800..39479246hg38UCSC Ensembl
chr15:39759013..39771434hg19UCSC Ensembl
Innerchr15:39759026..39771422hg19UCSC Ensembl
Outerchr15:39759001..39771447hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3812422
hg1912422
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636213
Supporting Variants
SamplesHG00473
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15226915
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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