A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486684



Internal ID21144237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62673282..62673660hg38UCSC Ensembl
chr14:63140000..63140378hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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