A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238774



Internal ID20805814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63424286..63424356hg38UCSC Ensembl
chr15:63716485..63716555hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238774
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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