A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578934



Internal ID20952005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80495565..80499459hg38UCSC Ensembl
chr17:78469365..78473259hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383895
hg193895
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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