A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434900



Internal ID21396902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:296001..383000hg38UCSC Ensembl
chr6:296001..383000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3887000
hg1987000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751234, nssv15753850, nssv15746066, nssv15748593
SamplesMDQ045, MDQ010, BTQ016, MDQ025
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434900
Frequency
Sample Size15
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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