A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588716



Internal ID20961787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70086734..70087732hg38UCSC Ensembl
chr17:68082875..68083873hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246088
Samples
Known GenesKCNJ16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588716
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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