A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950909



Internal ID22726302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42860164..42860164hg38UCSC Ensembl
chr3:42901656..42901656hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419896
Samples
Known GenesACKR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950909
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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