A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544317



Internal ID21868672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99875218..99885523hg38UCSC Ensembl
chr3:99594062..99604367hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3810306
hg1910306
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110539
Supporting Variants
Samples
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544317
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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