A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227275



Internal ID20794315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66057685..66979037hg38UCSC Ensembl
chr12:66451465..67372817hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38921353
hg19921353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581407
Supporting Variants
Samples
Known GenesGRIP1, HELB, IRAK3, LLPH, TMBIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227275
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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