A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494896



Internal ID21152449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86943011..86955054hg38UCSC Ensembl
chr14:87409355..87421398hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3812044
hg1912044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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