A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591124



Internal ID20964195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34957183..34958249hg38UCSC Ensembl
chr17:33284202..33285268hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381067
hg191067
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242130
Samples
Known GenesCCT6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591124
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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