A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636048



Internal ID6676157
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15204095, essv15204094, essv15204093, essv15204092, essv15204096
SamplesHG02571, HG02819, NA19788, HG02722, HG02464
Known GenesTRPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636048
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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