A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014186



Internal ID19103406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68422408..68530194hg38UCSC Ensembl
Innerchr4:69288126..69395912hg19UCSC Ensembl
Innerchr4:68970721..69078507hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38107787
hg19107787
hg18107787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5247n100
Supporting Variantsnssv3626878
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)nsv1014186
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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