A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945544



Internal ID31026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16442604..16459207hg38UCSC Ensembl
chr4:16444227..16460830hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3816604
hg1916604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443757
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945544
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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