A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010361



Internal ID19099578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68418861..68530736hg38UCSC Ensembl
Innerchr4:69284579..69396454hg19UCSC Ensembl
Innerchr4:68967174..69079049hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38111876
hg19111876
hg18111876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5247n100
Supporting Variantsnssv3740208
Samples
Known GenesTMPRSS11E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010361
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