A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600032



Internal ID16040755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151411732..151412904hg38UCSC Ensembl
Innerchr5:150791293..150792465hg19UCSC Ensembl
Innerchr5:150771486..150772658hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381173
hg191173
hg181173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10126n54
Supporting Variantsnssv1043706
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600032
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