A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505700



Internal ID20878973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67370558..67373958hg38UCSC Ensembl
chr16:67404461..67407861hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383401
hg193401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185731
Samples
Known GenesLRRC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505700
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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