A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523154



Internal ID15450447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79026016..79027922hg38UCSC Ensembl
Innerchr4:79947170..79949076hg19UCSC Ensembl
Innerchr4:80166194..80168100hg18UCSC Ensembl
Innerchr4:80304349..80306255hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg381907
hg191907
hg181907
hg171907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698862
Samples
Known GenesLINC01088
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523154
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