A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258683



Internal ID20825723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215389145..215389685hg38UCSC Ensembl
chr2:216253868..216254408hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539263
Supporting Variants
Samples
Known GenesFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258683
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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