A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582120



Internal ID16369529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61504343..61661567hg38UCSC Ensembl
Innerchr2:61731478..61888702hg19UCSC Ensembl
Innerchr2:61584982..61742206hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38157225
hg19157225
hg18157225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911334
Samples
Known GenesXPO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582120
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