A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489103



Internal ID21146656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74330524..74341531hg38UCSC Ensembl
chr14:74797227..74808234hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3811008
hg1911008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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