A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506509



Internal ID20879790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77992275..78060495hg38UCSC Ensembl
chr16:78026172..78094392hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3868221
hg1968221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2943n223
Supporting Variantsnssv18032062
Samples
Known GenesCLEC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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