A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010665



Internal ID6722755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89160398..89160465hg38UCSC Ensembl
chr16:89226806..89226873hg19UCSC Ensembl
chr16:87754307..87754374hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3868
hg1968
hg1868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3580515
SamplesHuRef
Known GenesLINC00304
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010665
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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