A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636044



Internal ID6676153
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15204086, essv15204088, essv15204087
SamplesHG01623, HG00365, HG02238
Known GenesTRPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636044
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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