A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583480



Internal ID20956551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62568475..62568842hg38UCSC Ensembl
chr17:60645836..60646203hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242589
Samples
Known GenesTLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583480
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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