A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948387



Internal ID32964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18997080..19049706hg38UCSC Ensembl
chr4:18998703..19051329hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3852627
hg1952627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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