A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239129



Internal ID20806169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97455385..97459333hg38UCSC Ensembl
chr15:97998615..98002563hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg383949
hg193949
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239129
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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