A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487719



Internal ID21145272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41902601..41981200hg38UCSC Ensembl
chr14:42371804..42450403hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3878600
hg1978600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181990
Samples
Known GenesLRFN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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