A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109441



Internal ID22018674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37437922..37437922hg38UCSC Ensembl
chr19:37928824..37928824hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628356
Samples
Known GenesZNF569
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109441
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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