A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559937



Internal ID20933008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22567498..22569122hg38UCSC Ensembl
chr4:22569121..22570745hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381625
hg191625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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