A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1412519



Internal ID12228956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22818880..22818933hg38UCSC Ensembl
chr16:22830201..22830254hg19UCSC Ensembl
chr16:22737702..22737755hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3613108
SamplesHuRef
Known GenesHS3ST2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1412519
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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