A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889283



Internal ID22664299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33471782..33472120hg38UCSC Ensembl
chr4:33473404..33473742hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889283
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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