A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583399



Internal ID20956470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57201189..57201926hg38UCSC Ensembl
chr17:55278550..55279287hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583399
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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