A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245288



Internal ID20812328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5414715..5415252hg38UCSC Ensembl
chr17:5318035..5318572hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575988
Supporting Variants
Samples
Known GenesNUP88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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