A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433828



Internal ID21395830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68732869..68775868hg38UCSC Ensembl
chr2:68960001..69003000hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3843000
hg1943000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751409
SamplesSMI041
Known GenesARHGAP25
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433828
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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