A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935214



Internal ID24198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97956730..97956730hg38UCSC Ensembl
chr3:97675574..97675574hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539192
Supporting Variants
Samples
Known GenesMINA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935214
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000163


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