A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484192



Internal ID21141745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73444350..73446448hg38UCSC Ensembl
chr14:73911058..73913156hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382099
hg192099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020162
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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