A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292952



Internal ID20502170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100203832..100206086hg38UCSC Ensembl
chr3:99922676..99924930hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg382255
hg192255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292952
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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