A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514779



Internal ID20888134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67814101..67836000hg38UCSC Ensembl
chr16:67848004..67869903hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3821900
hg1921900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188017
Samples
Known GenesCENPT, TSNAXIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514779
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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