A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582393



Internal ID16369802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89011066..90239257hg38UCSC Ensembl
Innerchr2:89310563..90278124hg19UCSC Ensembl
Innerchr2:89091678..89915429hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381228192
hg19967562
hg18823752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6949n54
Supporting Variantsnssv913922
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582393
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