A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947494



Internal ID32364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1844652..1845104hg38UCSC Ensembl
chr4:1846379..1846831hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442631
Supporting Variants
Samples
Known GenesLETM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947494
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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