A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584431



Internal ID20957502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19625806..19626258hg38UCSC Ensembl
chr16:19637128..19637580hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239190
Samples
Known GenesC16orf62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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