A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245279



Internal ID20812319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5388081..5389922hg38UCSC Ensembl
chr17:5291401..5293242hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381842
hg191842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581682
Supporting Variants
Samples
Known GenesNUP88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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