A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517829



Internal ID20891190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19213187..19215342hg38UCSC Ensembl
chr19:19323996..19326151hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382156
hg192156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198367
Samples
Known GenesNCAN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517829
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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