A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907702



Internal ID5915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111793475..111793475hg38UCSC Ensembl
chr1:112336097..112336097hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543982
Supporting Variants
Samples
Known GenesKCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907702
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002975


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