A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518353



Internal ID15445646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66385464..66396809hg38UCSC Ensembl
Innerchr1:66851147..66862492hg19UCSC Ensembl
Innerchr1:66623735..66635080hg18UCSC Ensembl
Innerchr1:66563168..66574513hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3811346
hg1911346
hg1811346
hg1711346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694063
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518353
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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