A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3576603



Internal ID6701299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89342073..89342076hg38UCSC Ensembl
chr16:89408481..89408484hg19UCSC Ensembl
chr16:87935982..87935985hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3891
hg1991
hg1891
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992694
Supporting Variants
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3576603
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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