A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629362



Internal ID21821409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35032833..35032833hg38UCSC Ensembl
chr17:33359852..33359852hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092585
Supporting Variants
Samples
Known GenesRAD51L3-RFFL, RFFL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629362
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