A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580183



Internal ID20953254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67126768..67127585hg38UCSC Ensembl
chr16:67160671..67161488hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243604
Samples
Known GenesC16orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580183
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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