A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3574650



Internal ID6699346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89566205..89566205hg38UCSC Ensembl
chr16:89632613..89632613hg19UCSC Ensembl
chr16:88160114..88160114hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3884
hg1984
hg1884
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994856
Supporting Variants
SamplesHuRef
Known GenesRPL13
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3574650
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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