A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703897



Internal ID127563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68281489..68281528hg38UCSC Ensembl
chr15:68573827..68573866hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541286
Supporting Variants
Samples
Known GenesFEM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703897
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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