A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567056



Internal ID20940127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2717067..2717542hg38UCSC Ensembl
chr4:2718794..2719269hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265002
Samples
Known GenesFAM193A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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