A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239064



Internal ID20806104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92893975..92894693hg38UCSC Ensembl
chr15:93437205..93437923hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578792
Supporting Variants
Samples
Known GenesLOC100507217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239064
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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