A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586499



Internal ID20959570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9637288..9638984hg38UCSC Ensembl
chr16:9731145..9732841hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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