A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583002



Internal ID20956073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55754226..55839537hg38UCSC Ensembl
chr16:55788138..55873449hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3885312
hg1985312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2882n223
Supporting Variantsnssv18239286
Samples
Known GenesCES1, CES1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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