A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496937



Internal ID20870140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57904702..57926451hg38UCSC Ensembl
chr16:57938606..57960355hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3821750
hg1921750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190392
Samples
Known GenesCNGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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