A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496930



Internal ID20870133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94029994..94030977hg38UCSC Ensembl
chr14:94496340..94497323hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38984
hg19984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022911
Samples
Known GenesOTUB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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