A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259784



Internal ID20469002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110120474..110120474hg38UCSC Ensembl
chr1:110663096..110663096hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382741
hg192741
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259784
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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