A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266142



Internal ID20833182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100587893..106707982hg38UCSC Ensembl
chr5:99923597..106043683hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg386120090
hg196120087
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567095
Supporting Variants
Samples
Known GenesC5orf30, GIN1, LINC00491, LINC00492, LOC102467212, NUDT12, PAM, PPIP5K2, RAB9BP1, SLCO4C1, SLCO6A1, ST8SIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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