A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484171



Internal ID21141724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41920124..41920466hg38UCSC Ensembl
chr14:42389327..42389669hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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