A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576397



Internal ID20949468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55751494..55886859hg38UCSC Ensembl
chr16:55785406..55920771hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38135366
hg19135366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239285
Samples
Known GenesCES1, CES1P1, CES5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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