A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586264



Internal ID7057646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57292346..57293295hg38UCSC Ensembl
Innerchr16:57326258..57327207hg19UCSC Ensembl
Innerchr16:55883759..55884708hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38950
hg19950
hg18950
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993464
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586264
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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