A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256357



Internal ID20823397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200886697..200887090hg38UCSC Ensembl
chr2:201751420..201751813hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548050
Supporting Variants
Samples
Known GenesPPIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256357
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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