A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433136



Internal ID21395138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4494941..4496940hg38UCSC Ensembl
chr1:4555001..4557000hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752347
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433136
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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