A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238763



Internal ID20805803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63124788..63125412hg38UCSC Ensembl
chr15:63416987..63417611hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578978
Supporting Variants
Samples
Known GenesLACTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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