A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265933



Internal ID20832973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69958517..69970420hg38UCSC Ensembl
chr4:70824235..70836138hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3811904
hg1911904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558121
Supporting Variants
Samples
Known GenesCSN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265933
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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