A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004426



Internal ID70588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141363791..141364904hg38UCSC Ensembl
chr7:141063591..141064704hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381114
hg191114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476587
Supporting Variants
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004426
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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