A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594884



Internal ID20967955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59214305..59392624hg38UCSC Ensembl
chr17:57291666..57469985hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38178320
hg19178320
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243731
Samples
Known GenesGDPD1, MIR4729, SMG8, YPEL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594884
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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