A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946641



Internal ID31787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26650371..26657744hg38UCSC Ensembl
chr4:26651993..26659366hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387374
hg197374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441861
Supporting Variants
Samples
Known GenesTBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946641
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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