A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577445



Internal ID20950516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65411283..65414711hg38UCSC Ensembl
chr17:63407401..63410829hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg383429
hg193429
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577445
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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