A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269138



Internal ID20478356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29093088..29093088hg38UCSC Ensembl
chr19:29583995..29583995hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269138
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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