A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15204095



Internal ID5205911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31155131..31159013hg38UCSC Ensembl
Innerchr15:31155131..31159013hg38UCSC Ensembl
Outerchr15:31154843..31159184hg38UCSC Ensembl
chr15:31447334..31451216hg19UCSC Ensembl
Innerchr15:31447334..31451216hg19UCSC Ensembl
Outerchr15:31447046..31451387hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383883
hg193883
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636048
Supporting Variants
SamplesHG02819
Known GenesTRPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15204095
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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