A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712155



Internal ID135821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21308158..21779798hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38471641
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712155
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.745083


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