A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101581



Internal ID22010814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46313828..46313828hg38UCSC Ensembl
chr19:46817085..46817085hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618518
Samples
Known GenesHIF3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101581
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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