A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269873



Internal ID20836913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161649493..166382472hg38UCSC Ensembl
chr6:162070525..166795960hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg384732980
hg194725436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556844
Supporting Variants
Samples
Known GenesC6orf118, CAHM, DKFZp451B082, LINC00473, LINC00602, LOC100289495, MPC1, PACRG, PACRG-AS1, PARK2, PDE10A, PRR18, QKI, SFT2D1, T
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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