A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584369



Internal ID20957440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38686509..38687250hg38UCSC Ensembl
chr17:36842762..36843503hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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