A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897015



Internal ID22672112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13291067..13297867hg38UCSC Ensembl
chr3:13332567..13339367hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386801
hg196801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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