A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568241



Internal ID20941312
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 StatusM
Merged Variants
Supporting Variantsnssv18264513
Samples
Known GenesASB5, SPATA4, WDR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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