A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244424



Internal ID20811464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32245967..32246448hg38UCSC Ensembl
chr17:30572986..30573467hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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