A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009408



Internal ID6721511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17132514..17132568hg38UCSC Ensembl
chr16:17226371..17226425hg19UCSC Ensembl
chr16:17133872..17133926hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3573351
SamplesHuRef
Known GenesXYLT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009408
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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