A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264513



Internal ID20831553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176156053..176227742hg38UCSC Ensembl
chr4:177077204..177148893hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3871690
hg1971690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568241
Supporting Variants
Samples
Known GenesASB5, SPATA4, WDR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264513
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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