A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1451902



Internal ID12268338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89454896..89454962hg38UCSC Ensembl
chr16:89521304..89521370hg19UCSC Ensembl
chr16:88048805..88048871hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4091058
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1451902
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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