A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597879



Internal ID16385288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41229175..41253751hg38UCSC Ensembl
Innerchr5:41229277..41253853hg19UCSC Ensembl
Innerchr5:41265034..41289610hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3824577
hg1924577
hg1824577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1029136
Samples
Known GenesC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597879
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