A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529745



Internal ID20903106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38620843..38641584hg38UCSC Ensembl
chr19:39111483..39132224hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3820742
hg1920742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198104
Samples
Known GenesEIF3K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529745
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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