A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264822



Internal ID20831862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147867872..147868380hg38UCSC Ensembl
chr4:148789023..148789531hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567638
Supporting Variants
Samples
Known GenesARHGAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264822
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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