A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109857



Internal ID22019090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32656103..32656103hg38UCSC Ensembl
chr19:33147009..33147009hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626206
Samples
Known GenesANKRD27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109857
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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