A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481455



Internal ID21139008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61166647..61166894hg38UCSC Ensembl
chr14:61633365..61633612hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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