A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945892



Internal ID31270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192501699..192529323hg38UCSC Ensembl
chr3:192219488..192247112hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3827625
hg1927625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449791
Supporting Variants
Samples
Known GenesFGF12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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