A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591643



Internal ID20964714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2535051..2676693hg38UCSC Ensembl
chr16:2585052..2726694hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38141643
hg19141643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242761
Samples
Known GenesERVK13-1, FLJ42627, LOC652276, PDPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591643
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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