A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588804



Internal ID20961875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67231578..67232172hg38UCSC Ensembl
chr17:65227694..65228288hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246049
Samples
Known GenesHELZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588804
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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