A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266157



Internal ID20833197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102278783..102279139hg38UCSC Ensembl
chr5:101614487..101614843hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559686
Supporting Variants
Samples
Known GenesSLCO4C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266157
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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