A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643619



Internal ID6683690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8567215..8586980hg38UCSC Ensembl
chr19:8632099..8651864hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3819766
hg1919766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15989225
SamplesNA18597
Known GenesADAMTS10, MYO1F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643619
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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