A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578972



Internal ID20952043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51026797..51027244hg38UCSC Ensembl
chr17:49104158..49104605hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245183
Samples
Known GenesSPAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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