A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588604



Internal ID20961675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67225984..67227440hg38UCSC Ensembl
chr17:65222100..65223556hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381457
hg191457
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246048
Samples
Known GenesHELZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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