A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957667



Internal ID39085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151499685..151500701hg38UCSC Ensembl
chr4:152420837..152421853hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472843
Supporting Variants
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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