A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv651814



Internal ID15041780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1757779..1835631hg38UCSC Ensembl
Innerchr16:1807780..1885632hg19UCSC Ensembl
Innerchr16:1747781..1825633hg18UCSC Ensembl
Innerchr16:1747781..1825633hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3877853
hg1977853
hg1877853
hg1777853
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517196
Supporting Variants
Samples
Known GenesEME2, FAHD1, HAGH, IGFALS, MAPK8IP3, MEIOB, MRPS34, NME3, NUBP2, SPSB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv651814
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