A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502292



Internal ID22560232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169098188..169106674hg38UCSC Ensembl
chr6:169498283..169506769hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388487
hg198487
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502292
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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