A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484212



Internal ID21141765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64355291..64359519hg38UCSC Ensembl
chr14:64822009..64826237hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg384229
hg194229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020690
Samples
Known GenesMIR548AZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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