A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579702



Internal ID20952773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31888921..31889568hg38UCSC Ensembl
chr17:30215940..30216587hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244396
Samples
Known GenesUTP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579702
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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