A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294973



Internal ID20504191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153217548..153217548hg38UCSC Ensembl
chr1:153190024..153190024hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294973
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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