A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056405



Internal ID21965638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34390668..34392831hg38UCSC Ensembl
chr19:34881573..34883736hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382164
hg192164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634285
Samples
Known GenesGPI
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056405
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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