A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636047



Internal ID6676156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31131859..31135920hg38UCSC Ensembl
Innerchr15:31131865..31135915hg38UCSC Ensembl
Outerchr15:31131854..31135926hg38UCSC Ensembl
chr15:31424062..31428123hg19UCSC Ensembl
Innerchr15:31424068..31428118hg19UCSC Ensembl
Outerchr15:31424057..31428129hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg384062
hg194062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15204091
SamplesHG04239
Known GenesTRPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636047
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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