A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525586



Internal ID15452879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:176255610..176307916hg38UCSC Ensembl
Innerchr1:176224746..176277052hg19UCSC Ensembl
Innerchr1:174491369..174543675hg18UCSC Ensembl
Innerchr1:172956403..173008709hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3852307
hg1952307
hg1852307
hg1752307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701725
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525586
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