A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575667



Internal ID20948738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49648828..49649519hg38UCSC Ensembl
chr17:47726190..47726881hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245145
Samples
Known GenesSPOP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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