A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510939



Internal ID20884262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3083045..3239935hg38UCSC Ensembl
chr16:3133046..3289935hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38156891
hg19156890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029190
Samples
Known GenesOR1F1, OR1F2P, ZNF200, ZNF205, ZNF205-AS1, ZNF213, ZSCAN10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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