A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524956



Internal ID15105563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:106733772..107575531hg38UCSC Ensembl
Innerchr13:107386120..108227879hg19UCSC Ensembl
Innerchr13:106184121..107025880hg18UCSC Ensembl
Innerchr13:106184121..107025880hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38841760
hg19841760
hg18841760
hg17841760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700977
Samples
Known GenesFAM155A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524956
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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