A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433854



Internal ID21395856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95036256..95041255hg38UCSC Ensembl
chr2:95702001..95707000hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749100
SamplesMDQ010
Known GenesMAL
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433854
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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