A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003227



Internal ID6715359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46409113..46409910hg38UCSC Ensembl
Innerchr10:47139841..47140638hg19UCSC Ensembl
Innerchr10:46559847..46560644hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38798
hg19798
hg18798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587037
SamplesHuRef
Known GenesLINC00842
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003227
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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