A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597260



Internal ID16384669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14871843..14872550hg38UCSC Ensembl
Innerchr5:14871952..14872659hg19UCSC Ensembl
Innerchr5:14924952..14925659hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38708
hg19708
hg18708
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1026064, nssv1026062, nssv1026063
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597260
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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