A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906650



Internal ID22681852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9795842..9796687hg38UCSC Ensembl
chr3:9837526..9838371hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424326
Samples
Known GenesARPC4, ARPC4-TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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