A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897513



Internal ID22672617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59385718..59385777hg38UCSC Ensembl
chr3:59371444..59371503hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897513
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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