A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564019



Internal ID20937090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169209345..169209821hg38UCSC Ensembl
chr4:170130496..170130972hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264372
Samples
Known GenesSH3RF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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