A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948862



Internal ID33265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38716207..38718777hg38UCSC Ensembl
chr4:38717828..38720398hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382571
hg192571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948862
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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