A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618057



Internal ID7004940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93469016..93484893hg38UCSC Ensembl
chr8:94481244..94497121hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3815878
hg1915878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13260183
SamplesNA19026
Known GenesLINC00535
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618057
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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