A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276315



Internal ID20485533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88957207..88957343hg38UCSC Ensembl
chr3:89006357..89006493hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734962
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276315
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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