A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958367



Internal ID39560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166755897..166761920hg38UCSC Ensembl
chr4:167677048..167683071hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386024
hg196024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455889
Supporting Variants
Samples
Known GenesSPOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.754685


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