A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557992



Internal ID18509587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16201938..16587029hg38UCSC Ensembl
Innerchr16:16295795..16680886hg19UCSC Ensembl
Innerchr16:16203296..16588387hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38385092
hg19385092
hg18385092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042492
Supporting Variants
Samples
Known GenesABCC6, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO3, NPIPA7, NPIPA8, PKD1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557992
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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