A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904599



Internal ID22679777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179633988..179634290hg38UCSC Ensembl
chr3:179351776..179352078hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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