A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268336



Internal ID20477554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150821823..150822165hg38UCSC Ensembl
chr3:150539610..150539952hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268336
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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