A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985363



Internal ID57649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89446569..89685113hg38UCSC Ensembl
chr6:90156288..90394832hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38238545
hg19238545
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457650
Supporting Variants
Samples
Known GenesANKRD6, LYRM2, MDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985363
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