A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1458e214



Internal ID22757352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17641247..17721211hg38UCSC Ensembl
chr9:17641245..17721209hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3879965
hg1979965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619851, esv3619850
SamplesNA20126, HG02107
Known GenesSH3GL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1458e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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