A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587073



Internal ID20960144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63396270..63396783hg38UCSC Ensembl
chr18:61063503..61064016hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245476
Samples
Known GenesVPS4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587073
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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