A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945196



Internal ID30796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12337916..12344958hg38UCSC Ensembl
chr4:12339540..12346582hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg387043
hg197043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945196
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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