A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240222



Internal ID20807262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44242224..44242913hg38UCSC Ensembl
chr15:44534422..44535111hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240222
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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