A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15204087



Internal ID5205903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31070206..31074094hg38UCSC Ensembl
Innerchr15:31070215..31074086hg38UCSC Ensembl
Outerchr15:31070198..31074103hg38UCSC Ensembl
chr15:31362409..31366297hg19UCSC Ensembl
Innerchr15:31362418..31366289hg19UCSC Ensembl
Outerchr15:31362401..31366306hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383889
hg193889
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636044
Supporting Variants
SamplesHG01623
Known GenesTRPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15204087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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