A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037433



Internal ID92709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68448995..68449018hg38UCSC Ensembl
chr10:70208752..70208775hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543367
Supporting Variants
Samples
Known GenesDNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037433
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.055937


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