A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498286



Internal ID20871495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1316425..1318839hg38UCSC Ensembl
chr16:1366426..1368840hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382415
hg192415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028763
Samples
Known GenesUBE2I
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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