A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238905



Internal ID20805945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65602093..65602534hg38UCSC Ensembl
chr15:65894431..65894872hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594459
Supporting Variants
Samples
Known GenesVWA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238905
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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