A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896182



Internal ID22671271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155402741..155406986hg38UCSC Ensembl
chr3:155120530..155124775hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384246
hg194246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896182
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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