A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1613886



Internal ID12430320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89196376..89196457hg38UCSC Ensembl
chr16:89262784..89262865hg19UCSC Ensembl
chr16:87790285..87790366hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3882
hg1982
hg1882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4272948
SamplesHuRef
Known GenesSLC22A31
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1613886
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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