A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573227



Internal ID20946298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169211393..169212287hg38UCSC Ensembl
chr4:170132544..170133438hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264374
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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