A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266085



Internal ID20833125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85514224..85515005hg38UCSC Ensembl
chr4:86435377..86436158hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567303
Supporting Variants
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266085
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00016


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