A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520477



Internal ID15447770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141519118..141522955hg38UCSC Ensembl
Innerchr4:142440271..142444108hg19UCSC Ensembl
Innerchr4:142659721..142663558hg18UCSC Ensembl
Innerchr4:142797876..142801713hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg383838
hg193838
hg183838
hg173838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697443
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520477
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