A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246091



Internal ID20813131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70465037..72981338hg38UCSC Ensembl
chr17:68461178..70977477hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg382516302
hg192516300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588977
Supporting Variants
Samples
Known GenesCASC17, LINC00511, LINC00673, SLC39A11, SOX9, SOX9-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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