A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515692



Internal ID15443303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31778861..31787274hg38UCSC Ensembl
Innerchr5:31778968..31787381hg19UCSC Ensembl
Innerchr5:31814725..31823138hg18UCSC Ensembl
Innerchr5:31814725..31823138hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg388414
hg198414
hg188414
hg178414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662026, nssv685521, nssv664437, nssv670721, nssv686686
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515692
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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