A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554057



Internal ID20927166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203303060..203303651hg38UCSC Ensembl
chr2:204167783..204168374hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257823
Samples
Known GenesCYP20A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554057
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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