A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894919



Internal ID22669995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181939350..181946945hg38UCSC Ensembl
chr3:181657138..181664733hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg387596
hg197596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894919
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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