A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635319



Internal ID18933600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167886977..168072721hg38UCSC Ensembl
Innerchr4:168808128..168993872hg19UCSC Ensembl
Innerchr4:169044703..169230447hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38185745
hg19185745
hg18185745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017771
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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