A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583614



Internal ID20956685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64495400..64496001hg38UCSC Ensembl
chr17:62491518..62492119hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243275
Samples
Known GenesPOLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer