A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478152



Internal ID22536053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35354313..35357496hg38UCSC Ensembl
chr17:33681332..33684515hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383184
hg193184
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877279
Supporting Variants
Samples
Known GenesSLFN11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478152
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