A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637562



Internal ID7024354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:261769..271795hg38UCSC Ensembl
chr16:311768..321794hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810027
hg1910027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355200, essv15355197, essv15355196, essv15355199, essv15355198, essv15355195
SamplesHG03095, NA19189, HG00376, NA19438, HG01105, NA19431
Known GenesITFG3, RGS11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637562
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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