A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582452



Internal ID16369861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:90379959..90399638hg38UCSC Ensembl
Innerchr2:91595887..91615566hg19UCSC Ensembl
Innerchr2:90959614..90979293hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg3819680
hg1919680
hg1819680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6962n54
Supporting Variantsnssv914034
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582452
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer