A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582265



Internal ID16369674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77760423..77814957hg38UCSC Ensembl
Innerchr2:77987549..78042083hg19UCSC Ensembl
Innerchr2:77841057..77895591hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3854535
hg1954535
hg1854535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6930n54
Supporting Variantsnssv913440
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582265
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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