A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697702



Internal ID121368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95169920..95169947hg38UCSC Ensembl
chr14:95636257..95636284hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540300
Supporting Variants
Samples
Known GenesDICER1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697702
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.075218


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer