A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548258



Internal ID20878715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203471362..203472136hg38UCSC Ensembl
chr2:204336085..204336859hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257838
Samples
Known GenesRAPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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