A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107768



Internal ID22017001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45732758..45732758hg38UCSC Ensembl
chr19:46236016..46236016hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382322
hg192322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107768
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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