A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273219



Internal ID20482437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16057002..16057002hg38UCSC Ensembl
chr2:16197124..16197124hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273219
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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