A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277049



Internal ID20486267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149245583..149251914hg38UCSC Ensembl
chr3:148963370..148969701hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg386332
hg196332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277049
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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