A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256061



Internal ID20823101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171446263..171447665hg38UCSC Ensembl
chr2:172302773..172304175hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549732
Supporting Variants
Samples
Known GenesDCAF17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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