A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589730



Internal ID20962801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47738647..47739521hg38UCSC Ensembl
chr17:45816013..45816887hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242495
Samples
Known GenesTBX21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589730
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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