A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526554



Internal ID15453847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:230286285..230287735hg38UCSC Ensembl
Innerchr1:230422031..230423481hg19UCSC Ensembl
Innerchr1:228488654..228490104hg18UCSC Ensembl
Innerchr1:226728766..226730216hg17UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381451
hg191451
hg181451
hg171451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702868
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526554
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