A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636112



Internal ID18587707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152324311..152378692hg38UCSC Ensembl
Innerchr4:153245463..153299844hg19UCSC Ensembl
Innerchr4:153464913..153519294hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3854382
hg1954382
hg1854382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024010
Supporting Variants
Samples
Known GenesDEAR, FBXW7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636112
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