A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588555



Internal ID20961626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48911336..48915992hg38UCSC Ensembl
chr16:48945247..48949903hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg384657
hg194657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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