A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563861



Internal ID7034961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:11585162..11593432hg38UCSC Ensembl
Outerchr16:11679018..11687288hg19UCSC Ensembl
Outerchr16:11586519..11594789hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg388271
hg198271
hg188271
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991827
Supporting Variants
SamplesHuRef
Known GenesLITAF
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563861
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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