A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280626



Internal ID20847666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36268995..36269893hg38UCSC Ensembl
chr9:36268992..36269890hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38899
hg19899
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564284
Supporting Variants
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280626
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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