A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699829



Internal ID123495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55955019..55955026hg38UCSC Ensembl
chr15:56247217..56247224hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544993
Supporting Variants
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.023572


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