A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586975



Internal ID6711671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10056269..10057322hg38UCSC Ensembl
Innerchr16:10150126..10151179hg19UCSC Ensembl
Innerchr16:10057627..10058680hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381054
hg191054
hg181054
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005648
Supporting Variants
SamplesHuRef
Known GenesGRIN2A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586975
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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