A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257122



Internal ID20824163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197642708..197643385hg38UCSC Ensembl
chr2:198507432..198508109hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539080
Supporting Variants
Samples
Known GenesRFTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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