A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573241



Internal ID20946312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108626458..108626748hg38UCSC Ensembl
chr4:109547614..109547904hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262958
Samples
Known GenesRPL34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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