A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559984



Internal ID18511579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88228010..88560181hg38UCSC Ensembl
Innerchr16:88261616..88626589hg19UCSC Ensembl
Innerchr16:86819117..87154090hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38332172
hg19364974
hg18334974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061590
Supporting Variants
Samples
Known GenesMIR5189, ZFPM1, ZNF469
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559984
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