A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900941



Internal ID22676088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143423998..143430744hg38UCSC Ensembl
chr3:143142840..143149586hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg386747
hg196747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402365
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900941
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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