A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595558



Internal ID20968629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62437864..62439327hg38UCSC Ensembl
chr17:60515225..60516688hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381464
hg191464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242582
Samples
Known GenesMETTL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595558
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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