A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270155



Internal ID20837195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20461002..20462639hg38UCSC Ensembl
chr6:20461233..20462870hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381638
hg191638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565560
Supporting Variants
Samples
Known GenesE2F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270155
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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