A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239125



Internal ID20806165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96850681..96875631hg38UCSC Ensembl
chr15:97393911..97418861hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3824951
hg1924951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239125
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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