A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279319



Internal ID20846359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100541752..100545110hg38UCSC Ensembl
chr9:103304034..103307392hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg383359
hg193359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572913
Supporting Variants
Samples
Known GenesMSANTD3-TMEFF1, TMEFF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279319
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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