A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270498



Internal ID20837538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160100808..163436611hg38UCSC Ensembl
chr6:160521840..163857643hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383335804
hg193335804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567260
Supporting Variants
Samples
Known GenesAGPAT4, AGPAT4-IT1, CAHM, DKFZp451B082, IGF2R, LPA, LPAL2, MAP3K4, PACRG, PACRG-AS1, PARK2, PLG, QKI, SLC22A1, SLC22A2, SLC22A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270498
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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