A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270258



Internal ID20837298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78185642..78186280hg38UCSC Ensembl
chr5:77481466..77482104hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560301
Supporting Variants
Samples
Known GenesAP3B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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