A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1457e214



Internal ID22757351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17581661..17636018hg38UCSC Ensembl
chr9:17581659..17636016hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3854358
hg1954358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619847, esv3619848
SamplesNA12287, HG00263, HG00157
Known GenesSH3GL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1457e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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