A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527400



Internal ID8421675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:111073803..111083327hg38UCSC Ensembl
Innerchr10:112833561..112843085hg19UCSC Ensembl
Innerchr10:112823551..112833075hg18UCSC Ensembl
Innerchr10:112823551..112833075hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg389525
hg199525
hg189525
hg179525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703836
Samples
Known GenesADRA2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527400
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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