A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655361



Internal ID15045327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1729694..1804539hg38UCSC Ensembl
Innerchr16:1779695..1854540hg19UCSC Ensembl
Innerchr16:1719696..1794541hg18UCSC Ensembl
Innerchr16:1719696..1794541hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3874846
hg1974846
hg1874846
hg1774846
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517196
Supporting Variants
Samples
Known GenesEME2, IGFALS, MAPK8IP3, MIR3177, MRPS34, NME3, NUBP2, SPSB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655361
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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