A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589705



Internal ID20962776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72281441..73560584hg38UCSC Ensembl
chr16:72315340..73594483hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg381279144
hg191279144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240730
Samples
Known GenesC16orf47, HCCAT5, LOC100506172, ZFHX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589705
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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