A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668951



Internal ID15058917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1757779..1789022hg38UCSC Ensembl
Innerchr16:1807780..1839023hg19UCSC Ensembl
Innerchr16:1747781..1779024hg18UCSC Ensembl
Innerchr16:1747781..1779024hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3831244
hg1931244
hg1831244
hg1731244
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517196
Supporting Variants
Samples
Known GenesEME2, MAPK8IP3, MRPS34, NME3, NUBP2, SPSB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668951
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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