A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894587



Internal ID22669660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127264667..127264788hg38UCSC Ensembl
chr3:126983510..126983631hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894587
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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