A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591574



Internal ID20964645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64478723..64479320hg38UCSC Ensembl
chr17:62474840..62475437hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243273
Samples
Known GenesPOLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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