A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294561



Internal ID20503779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57435214..57435214hg38UCSC Ensembl
chr19:57946582..57946582hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294561
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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