A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103649



Internal ID22012883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36222838..36222838hg38UCSC Ensembl
chr19:36713740..36713740hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621086
Samples
Known GenesZNF146
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103649
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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