A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050662



Internal ID21959895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29010105..29010185hg38UCSC Ensembl
chr19:29501012..29501092hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619059
Samples
Known GenesLOC100505835
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050662
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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