A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591241



Internal ID20964312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64483300..64483846hg38UCSC Ensembl
chr17:62479417..62479963hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243274
Samples
Known GenesPOLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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