A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527494



Internal ID15108101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150944370..150959613hg38UCSC Ensembl
Innerchr4:151865522..151880765hg19UCSC Ensembl
Innerchr4:152084972..152100215hg18UCSC Ensembl
Innerchr4:152223127..152238370hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3815244
hg1915244
hg1815244
hg1715244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703942
Samples
Known GenesLRBA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527494
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