A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560862



Internal ID20933933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148850328..148851062hg38UCSC Ensembl
chr3:148568115..148568849hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5053n223
Supporting Variantsnssv18262569
Samples
Known GenesCPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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