A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522757



Internal ID15103364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151548255..151549457hg38UCSC Ensembl
Innerchr1:151520731..151521933hg19UCSC Ensembl
Innerchr1:149787355..149788557hg18UCSC Ensembl
Innerchr1:148333804..148335006hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381203
hg191203
hg181203
hg171203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698396
Samples
Known GenesTUFT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522757
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