A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576594



Internal ID20949665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39361726..39362841hg38UCSC Ensembl
chr17:37517979..37519094hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3105n223
Supporting Variantsnssv18242907
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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