A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889157



Internal ID22664171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24704039..24779036hg38UCSC Ensembl
chr3:24745530..24820527hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3874998
hg1974998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889157
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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