A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594864



Internal ID20967935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69896417..69897412hg38UCSC Ensembl
chr17:67892558..67893553hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38996
hg19996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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