A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506984



Internal ID20880272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67315407..67315740hg38UCSC Ensembl
chr16:67349310..67349643hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181864
Samples
Known GenesKCTD19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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