A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407782



Internal ID22465652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129596836..129596906hg38UCSC Ensembl
chr3:129315679..129315749hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899369
Supporting Variants
Samples
Known GenesPLXND1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407782
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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