A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494856



Internal ID21152409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87829501..87884600hg38UCSC Ensembl
chr14:88295845..88350944hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3855100
hg1955100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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