A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274613



Internal ID20483831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9802404..9802515hg38UCSC Ensembl
chr3:9844088..9844199hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734197
Supporting Variants
Samples
Known GenesARPC4, ARPC4-TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274613
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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