A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525860



Internal ID15106467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:129145535..129499413hg38UCSC Ensembl
InnerchrX:128279512..128633390hg19UCSC Ensembl
InnerchrX:128107193..128461071hg18UCSC Ensembl
InnerchrX:128005047..128358925hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38353879
hg19353879
hg18353879
hg17353879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702056
Samples
Known GenesSMARCA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525860
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