A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044742



Internal ID97575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19663867..19663917hg38UCSC Ensembl
chr11:19685413..19685463hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547237
Supporting Variants
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044742
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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