A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954209



Internal ID36802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97653930..97809420hg38UCSC Ensembl
chr4:98575081..98730571hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38155491
hg19155491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473731
Supporting Variants
Samples
Known GenesSTPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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