A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713367



Internal ID137033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45360601..45364317hg38UCSC Ensembl
chr17:43437967..43441683hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg383717
hg193717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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