A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586931



Internal ID20960002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72967646..72968752hg38UCSC Ensembl
chr16:73001545..73002651hg19UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240743
Samples
Known GenesZFHX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586931
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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