A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495602



Internal ID20868796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104495243..104586301hg38UCSC Ensembl
chr14:104961580..105052638hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3891059
hg1991059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189867
Samples
Known GenesC14orf180
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495602
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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