A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636260



Internal ID6676369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42129273..42141661hg38UCSC Ensembl
Innerchr15:42129323..42141328hg38UCSC Ensembl
Outerchr15:42129036..42141898hg38UCSC Ensembl
chr15:42421471..42433859hg19UCSC Ensembl
Innerchr15:42421521..42433526hg19UCSC Ensembl
Outerchr15:42421234..42434096hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3812389
hg1912389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230820, essv15230806, essv15230808, essv15230819, essv15230812, essv15230818, essv15230815, essv15230814, essv15230813, essv15230811, essv15230809, essv15230807, essv15230810, essv15230817, essv15230805, essv15230816
SamplesNA19066, HG01855, NA18979, NA19005, NA18993, NA18970, HG02082, HG01867, NA19082, NA18991, NA18939, HG01845, NA18946, NA18952, NA19072, HG02028
Known GenesPLA2G4F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636260
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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