A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1506985



Internal ID12323421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89421265..89421415hg38UCSC Ensembl
chr16:89487673..89487823hg19UCSC Ensembl
chr16:88015174..88015324hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38151
hg19151
hg18151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3763769
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1506985
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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