A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892440



Internal ID22667491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57573624..57573984hg38UCSC Ensembl
chr3:57559351..57559711hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417945
Samples
Known GenesARF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892440
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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