A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256041



Internal ID20823081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200326854..200327140hg38UCSC Ensembl
chr2:201191577..201191863hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548697
Supporting Variants
Samples
Known GenesSPATS2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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