A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15204090



Internal ID5205906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31078810..31084139hg38UCSC Ensembl
Innerchr15:31078810..31084139hg38UCSC Ensembl
Outerchr15:31078623..31084308hg38UCSC Ensembl
chr15:31371013..31376342hg19UCSC Ensembl
Innerchr15:31371013..31376342hg19UCSC Ensembl
Outerchr15:31370826..31376511hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg385330
hg195330
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636046
Supporting Variants
SamplesHG01566
Known GenesTRPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15204090
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer