A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592967



Internal ID20966038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65620606..65623164hg38UCSC Ensembl
chr17:63616724..63619282hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3230n223
Supporting Variantsnssv18245999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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