A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551519



Internal ID15992242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73873821..73874851hg38UCSC Ensembl
Innerchr10:75633579..75634609hg19UCSC Ensembl
Innerchr10:75303585..75304615hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381031
hg191031
hg181031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1264n54
Supporting Variantsnssv750277
Samples
Known GenesCAMK2G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551519
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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