A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091265



Internal ID22000498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72685371..72685371hg38UCSC Ensembl
chr17:70681510..70681510hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620087
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091265
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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