A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267184



Internal ID20834224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112278272..112279065hg38UCSC Ensembl
chr5:111613969..111614762hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567114
Supporting Variants
Samples
Known GenesEPB41L4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267184
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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