A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576400



Internal ID20949471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84149691..84150622hg38UCSC Ensembl
chr16:84183296..84184227hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240863
Samples
Known GenesDNAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576400
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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