A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244551



Internal ID20811591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72714084..72715719hg38UCSC Ensembl
chr17:70710223..70711858hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381636
hg191636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593546
Supporting Variants
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244551
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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