A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505379



Internal ID20878648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65484076..65502987hg38UCSC Ensembl
chr16:65517979..65536890hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3818912
hg1918912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178416
Samples
Known GenesLINC00922
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505379
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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