A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267217



Internal ID20834257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113381751..113382307hg38UCSC Ensembl
chr5:112717448..112718004hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574089
Supporting Variants
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267217
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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