A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15231141



Internal ID6295960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43176675..43178191hg38UCSC Ensembl
Innerchr15:43176725..43178133hg38UCSC Ensembl
Outerchr15:43176598..43178268hg38UCSC Ensembl
chr15:43468873..43470389hg19UCSC Ensembl
Innerchr15:43468923..43470331hg19UCSC Ensembl
Outerchr15:43468796..43470466hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381517
hg191517
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636288
Supporting Variants
SamplesNA19900
Known GenesTMEM62
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15231141
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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