A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243369



Internal ID20810409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9312248..9312972hg38UCSC Ensembl
chr17:9215565..9216289hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588340
Supporting Variants
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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