A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583909



Internal ID20956980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49772815..49776014hg38UCSC Ensembl
chr16:49806726..49809925hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240678
Samples
Known GenesZNF423
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583909
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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