A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586706



Internal ID20959777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21122583..21123962hg38UCSC Ensembl
chr17:21025896..21027275hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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