A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483343



Internal ID21140896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62448531..62524804hg38UCSC Ensembl
chr14:62915249..62991522hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3876274
hg1976274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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