A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902520



Internal ID22677679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114104040..114104109hg38UCSC Ensembl
chr3:113822887..113822956hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902520
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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