A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284397



Internal ID20493615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13658364..13658364hg38UCSC Ensembl
chr1:13984859..13984859hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284397
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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