A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636928



Internal ID7023722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75718175..75719634hg38UCSC Ensembl
Innerchr15:75718206..75719604hg38UCSC Ensembl
Outerchr15:75718145..75719665hg38UCSC Ensembl
chr15:76010516..76011975hg19UCSC Ensembl
Innerchr15:76010547..76011945hg19UCSC Ensembl
Outerchr15:76010486..76012006hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15293108, essv15293110, essv15293107, essv15293109
SamplesNA18910, HG01241, HG03084, NA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636928
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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