A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480163



Internal ID21137716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48275232..48393908hg38UCSC Ensembl
chr14:48744435..48863111hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38118677
hg19118677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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