A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896286



Internal ID22671376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134643144..134643208hg38UCSC Ensembl
chr3:134361986..134362050hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397077
Samples
Known GenesKY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896286
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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