A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496260



Internal ID20869460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58600140..58604930hg38UCSC Ensembl
chr16:58634044..58638834hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384791
hg194791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030862
Samples
Known GenesCNOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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