A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586658



Internal ID20959729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34953482..34953924hg38UCSC Ensembl
chr17:33280501..33280943hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242129
Samples
Known GenesCCT6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586658
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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