A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270174



Internal ID20837214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20783933..20784500hg38UCSC Ensembl
chr6:20784164..20784731hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570882
Supporting Variants
Samples
Known GenesCDKAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270174
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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