A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566053



Internal ID20939124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137031692..137261517hg38UCSC Ensembl
chr4:137952846..138182671hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38229826
hg19229826
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566053
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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