A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690864



Internal ID18642459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144923810..145028543hg38UCSC Ensembl
Innerchr8:146149196..146253929hg19UCSC Ensembl
Innerchr8:146120000..146224733hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38104734
hg19104734
hg18104734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032588
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)nssv3690864
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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