A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005648



Internal ID6717768
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586975
SamplesHuRef
Known GenesGRIN2A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005648
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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