A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975143



Internal ID50817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145862168..145862472hg38UCSC Ensembl
chr5:145241731..145242035hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470898
Supporting Variants
Samples
Known GenesGRXCR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975143
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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