A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896431



Internal ID22671524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184127016..184128880hg38UCSC Ensembl
chr3:183844804..183846668hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381865
hg191865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896431
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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