A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268519



Internal ID20477737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204375908..204375908hg38UCSC Ensembl
chr1:204345036..204345036hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268519
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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