A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591019



Internal ID20964090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48939075..48939615hg38UCSC Ensembl
chr17:47016437..47016977hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244488
Samples
Known GenesSNF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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