A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975581



Internal ID51112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148021659..148360000hg38UCSC Ensembl
chr5:147401222..147739563hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38338342
hg19338342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457815
Supporting Variants
Samples
Known GenesLOC102546294, SPINK13, SPINK14, SPINK5, SPINK6, SPINK7, SPINK9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975581
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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