A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270535



Internal ID20837575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3004611..3051208hg38UCSC Ensembl
chr6:3004845..3051442hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3846598
hg1946598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563981
Supporting Variants
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270535
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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