A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479011



Internal ID21136564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34347322..34435602hg38UCSC Ensembl
chr14:34816528..34904808hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3888281
hg1988281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179979
Samples
Known GenesSPTSSA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479011
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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