A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896271



Internal ID22671361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31351464..31351531hg38UCSC Ensembl
chr4:31353086..31353153hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896271
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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