A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889714



Internal ID22664734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194576579..194576712hg38UCSC Ensembl
chr3:194297308..194297441hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889714
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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