A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734409



Internal ID20510344
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 StatusM
Merged Variants
Supporting Variantsnssv16281158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734409
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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