A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271214



Internal ID20838254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33556987..33558195hg38UCSC Ensembl
chr6:33524764..33525972hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381209
hg191209
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559293
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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