A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897791



Internal ID22672898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157621484..157625337hg38UCSC Ensembl
chr3:157339273..157343126hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg383854
hg193854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897791
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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