A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479076



Internal ID21136629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55668733..55755810hg38UCSC Ensembl
chr14:56135451..56222528hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3887078
hg1987078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181337
Samples
Known GenesKTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479076
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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