A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872074



Internal ID22647012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32599517..32601273hg38UCSC Ensembl
chr1:33065118..33066874hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381757
hg191757
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386932
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872074
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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