A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271810



Internal ID20481028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45648253..45648253hg38UCSC Ensembl
chr19:46151511..46151511hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271810
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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