A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271527



Internal ID20838567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53559554..53559947hg38UCSC Ensembl
chr6:53424352..53424745hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556640
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271527
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00035


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