A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245316



Internal ID20812356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55621680..55628368hg38UCSC Ensembl
chr17:53699041..53705729hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg386689
hg196689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578533
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245316
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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