A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586941



Internal ID20960012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55762607..55831110hg38UCSC Ensembl
chr16:55796519..55865022hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3868504
hg1968504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2882n223
Supporting Variantsnssv18239289
Samples
Known GenesCES1, CES1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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