A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258996



Internal ID20826036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73129132..73261935hg38UCSC Ensembl
chr2:73356260..73489063hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38132804
hg19132804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544990
Supporting Variants
Samples
Known GenesCCT7, FBXO41, NOTO, PRADC1, SMYD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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