A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433143



Internal ID21395145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55935503..55935860hg38UCSC Ensembl
chr1:56401176..56401533hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750648
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433143
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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