A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690868



Internal ID18989149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144926067..145021974hg38UCSC Ensembl
Innerchr8:146151453..146247360hg19UCSC Ensembl
Innerchr8:146122257..146218164hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3895908
hg1995908
hg1895908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016357
Supporting Variants
Samples
Known GenesTMED10P1, ZNF16, ZNF252P, ZNF252P-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690868
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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