A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526080



Internal ID15106687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1132638..1152657hg38UCSC Ensembl
Innerchr19:1132637..1152656hg19UCSC Ensembl
Innerchr19:1083637..1103656hg18UCSC Ensembl
Innerchr19:1083637..1103656hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3820020
hg1920020
hg1820020
hg1720020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702324
Samples
Known GenesSBNO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526080
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