A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242994



Internal ID20810034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42318149..42319061hg38UCSC Ensembl
chr17:40470167..40471079hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582391
Supporting Variants
Samples
Known GenesSTAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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