A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238992



Internal ID20806032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42309541..42309812hg38UCSC Ensembl
chr15:42601739..42602010hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586568
Supporting Variants
Samples
Known GenesGANC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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