A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047330



Internal ID21956563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57017308..57018058hg38UCSC Ensembl
chr19:57528676..57529426hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047330
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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