A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433046



Internal ID21395048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222377020..222377916hg38UCSC Ensembl
chr1:222550362..222551258hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv49n172
Supporting Variantsnssv15752555
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433046
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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