A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516604



Internal ID15443897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20472407..20472639hg38UCSC Ensembl
Innerchr16:20483729..20483961hg19UCSC Ensembl
Innerchr16:20391230..20391462hg18UCSC Ensembl
Innerchr16:20391230..20391462hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38233
hg19233
hg18233
hg17233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676418, nssv669505
Samples
Known GenesACSM2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516604
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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