A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427879



Internal ID22485749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31677786..31678105hg38UCSC Ensembl
chr3:31719278..31719597hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905063
Supporting Variants
Samples
Known GenesOSBPL10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427879
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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