A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732908



Internal ID156574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50914514..50914565hg38UCSC Ensembl
chr20:49531051..49531102hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416596
Supporting Variants
Samples
Known GenesADNP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732908
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