A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577928



Internal ID20950999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66258267..66260091hg38UCSC Ensembl
chr16:66292170..66293994hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381825
hg191825
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577928
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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