A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238745



Internal ID20805785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23666442..23667083hg38UCSC Ensembl
chr15:23911589..23912230hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588379
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238745
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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