A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593459



Internal ID20966530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67740087..67741070hg38UCSC Ensembl
chr17:65736203..65737186hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38984
hg19984
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243793
Samples
Known GenesNOL11, SNORA38B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593459
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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