A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946799



Internal ID31886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33705103..33712383hg38UCSC Ensembl
chr4:33706725..33714005hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg387281
hg197281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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