A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590223



Internal ID20963294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65052213..65053026hg38UCSC Ensembl
chr17:63048331..63049144hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243312
Samples
Known GenesGNA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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