A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483985



Internal ID21141538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21888498..22496897hg38UCSC Ensembl
chr14:22356678..22965882hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38608400
hg19609205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2060n223
Supporting Variantsnssv18016059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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