A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1439e214



Internal ID22757333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9798117..9828748hg38UCSC Ensembl
chr9:9798117..9828748hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3830632
hg1930632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619527, esv3619526
SamplesNA20802, HG01524, NA11840
Known GenesPTPRD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1439e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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