A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635608



Internal ID18587203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183654315..183946499hg38UCSC Ensembl
Innerchr4:184575468..184867652hg19UCSC Ensembl
Innerchr4:184812462..185104646hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38292185
hg19292185
hg18292185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025333
Supporting Variants
Samples
Known GenesRWDD4, STOX2, TRAPPC11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635608
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