A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948209



Internal ID32838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13834891..13834956hg38UCSC Ensembl
chr4:13836515..13836580hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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