A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898500



Internal ID22673616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101680713..101680778hg38UCSC Ensembl
chr3:101399557..101399622hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898500
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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