A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481464



Internal ID21139017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70654450..70655251hg38UCSC Ensembl
chr14:71121167..71121968hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187081
Samples
Known GenesTTC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481464
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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