A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281158



Internal ID20490376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174484236..174484551hg38UCSC Ensembl
chr3:174202026..174202341hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281158
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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