A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582266



Internal ID16369675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77762481..77801430hg38UCSC Ensembl
Innerchr2:77989607..78028556hg19UCSC Ensembl
Innerchr2:77843115..77882064hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3838950
hg1938950
hg1838950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6930n54
Supporting Variantsnssv913441
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582266
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