A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952781



Internal ID35873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94269119..94270099hg38UCSC Ensembl
chr4:95190270..95191250hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468481
Supporting Variants
Samples
Known GenesSMARCAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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