A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619804



Internal ID7006678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16058917..16096870hg38UCSC Ensembl
chr9:16058915..16096868hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3837954
hg1937954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1455e214
Supporting Variantsessv13409953, essv13409952, essv13409954, essv13409951
SamplesNA19355, HG02070, NA18981, NA19434
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619804
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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