A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950864



Internal ID34608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46741688..46741873hg38UCSC Ensembl
chr4:46743705..46743890hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461804
Supporting Variants
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950864
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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