A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734875



Internal ID20510815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109384449..109386097hg38UCSC Ensembl
chr3:109103296..109104944hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381649
hg191649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734875
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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