A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544967



Internal ID20918205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197657506..197658008hg38UCSC Ensembl
chr2:198522230..198522732hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257123
Samples
Known GenesRFTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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