A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043940



Internal ID97023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42186990..42186990hg38UCSC Ensembl
chr11:42208540..42208540hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043940
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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