A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526528



Internal ID15453821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89081456..89087918hg38UCSC Ensembl
Innerchr1:89547139..89553601hg19UCSC Ensembl
Innerchr1:89319727..89326189hg18UCSC Ensembl
Innerchr1:89259160..89265622hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg386463
hg196463
hg186463
hg176463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702841
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526528
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