A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586039



Internal ID20959110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17687869..17688721hg38UCSC Ensembl
chr17:17591183..17592035hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242092
Samples
Known GenesRAI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586039
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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