A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592186



Internal ID20965257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29510371..29511404hg38UCSC Ensembl
chr17:27837389..27838422hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241696
Samples
Known GenesTAOK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592186
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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