A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549971



Internal ID15990694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12448787..12457861hg38UCSC Ensembl
Innerchr10:12490786..12499860hg19UCSC Ensembl
Innerchr10:12530792..12539866hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg389075
hg199075
hg189075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744011
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549971
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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