A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581473



Internal ID20954544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64646906..64649329hg38UCSC Ensembl
chr16:64680809..64683232hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382424
hg192424
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581473
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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