A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959689



Internal ID40430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183562983..183566925hg38UCSC Ensembl
chr4:184484136..184488078hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg383943
hg193943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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