A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056296



Internal ID21965529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29494309..29494885hg38UCSC Ensembl
chr19:29985216..29985792hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630422
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056296
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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