A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589748



Internal ID20962819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31464420..31465836hg38UCSC Ensembl
chr17:29791438..29792854hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242454
Samples
Known GenesRAB11FIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589748
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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