A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715926



Internal ID139592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3536936..3536987hg38UCSC Ensembl
chr18:3536934..3536985hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417137
Supporting Variants
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715926
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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