A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13569806



Internal ID5231467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94486938..94547326hg38UCSC Ensembl
chr9:97249220..97309608hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3860389
hg1960389
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621125
Supporting Variants
SamplesNA18626
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13569806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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