A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243225



Internal ID20810265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77068980..77096473hg38UCSC Ensembl
chr17:75065062..75092555hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3827494
hg1927494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584771
Supporting Variants
Samples
Known GenesLINC00338, MIR6516, SCARNA16, SEC14L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243225
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00136


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