A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517423



Internal ID20890784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41550866..41670990hg38UCSC Ensembl
chr19:42057234..42174918hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38120125
hg19117685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198815
Samples
Known GenesCEACAM21, CEACAM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517423
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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