A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156178



Internal ID22086683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68494770..68655691hg38UCSC Ensembl
Outerchr4:68478894..68663241hg38UCSC Ensembl
Innerchr4:69360488..69521409hg19UCSC Ensembl
Outerchr4:69344612..69528959hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38184348
hg19184348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv218n97
Supporting Variantsnssv4016701
Samples
Known GenesTMPRSS11E, UGT2B15, UGT2B17
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156178
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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