A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516966



Internal ID15097573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127260261..127277127hg38UCSC Ensembl
Innerchr9:130022540..130039406hg19UCSC Ensembl
Innerchr9:129062361..129079227hg18UCSC Ensembl
Innerchr9:127102094..127118960hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3816867
hg1916867
hg1816867
hg1716867
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653844, nssv692573, nssv655598, nssv653525, nssv664752, nssv669396, nssv657520, nssv685062, nssv662788, nssv668871, nssv687469, nssv675043, nssv680181, nssv677761, nssv678208, nssv690028, nssv679818
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516966
Frequency
Sample Size2026
Observed Gain4
Observed Loss13
Observed Complex0
Frequencyn/a


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