A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735012



Internal ID158678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174265026..174274885hg38UCSC Ensembl
chr3:173982816..173992675hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg389860
hg199860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442703
Supporting Variants
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735012
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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