A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022872



Internal ID82944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38084662..38084833hg38UCSC Ensembl
chr9:38084659..38084830hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022872
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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