A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13402186



Internal ID568872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10647445..10706472hg38UCSC Ensembl
chr9:10647445..10706472hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3859028
hg1959028
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619561
Supporting Variants
SamplesHG00250
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13402186
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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