A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108522



Internal ID22017755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31199764..31199764hg38UCSC Ensembl
chr19:31690670..31690670hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108522
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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