A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15317047



Internal ID3591384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89005704..89008312hg38UCSC Ensembl
Innerchr15:89005714..89008302hg38UCSC Ensembl
Outerchr15:89005694..89008322hg38UCSC Ensembl
chr15:89548935..89551543hg19UCSC Ensembl
Innerchr15:89548945..89551533hg19UCSC Ensembl
Outerchr15:89548925..89551553hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382609
hg192609
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637180
Supporting Variants
SamplesHG03175
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15317047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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