A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554463



Internal ID20927557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20107030..20107531hg38UCSC Ensembl
chr3:20148522..20149023hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4811n223
Supporting Variantsnssv18261914
Samples
Known GenesKAT2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554463
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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