A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901104



Internal ID22676252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104151378..104151969hg38UCSC Ensembl
chr3:103870222..103870813hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901104
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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