A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998101



Internal ID7081504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:19171288..19184549hg38UCSC Ensembl
Outerchr16:19182610..19195871hg19UCSC Ensembl
Outerchr16:19090111..19103372hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3813262
hg1913262
hg1813262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564793
SamplesHuRef
Known GenesSYT17
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998101
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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