A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978584



Internal ID53095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169776141..169776207hg38UCSC Ensembl
chr5:169203145..169203211hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462508
Supporting Variants
Samples
Known GenesDOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978584
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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