A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620984



Internal ID6661165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87712728..87720643hg38UCSC Ensembl
chr9:90327643..90335558hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387916
hg197916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13548023
SamplesNA20851
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620984
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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