A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531074



Internal ID20904435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41882510..41882994hg38UCSC Ensembl
chr19:42386577..42387061hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531074
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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