A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538720



Internal ID20912034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203254180..203254519hg38UCSC Ensembl
chr2:204118903..204119242hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257813
Samples
Known GenesCYP20A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538720
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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