A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563732



Internal ID7036492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1223866..1257851hg38UCSC Ensembl
Outerchr16:1273866..1307852hg19UCSC Ensembl
Outerchr16:1213867..1247853hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3833986
hg1933987
hg1833987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000058
Supporting Variants
SamplesHuRef
Known GenesTPSAB1, TPSB2, TPSD1, TPSG1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563732
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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