A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517734



Internal ID15445027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:173178124..173184645hg38UCSC Ensembl
Innerchr5:172605127..172611648hg19UCSC Ensembl
Innerchr5:172537733..172544254hg18UCSC Ensembl
Innerchr5:172537733..172544254hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg386522
hg196522
hg186522
hg176522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679444, nssv653043, nssv656340
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517734
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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