A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580596



Internal ID20953667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29520274..29520472hg38UCSC Ensembl
chr17:27847292..27847490hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241702
Samples
Known GenesTAOK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580596
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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