A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549974



Internal ID15990697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12526167..12535794hg38UCSC Ensembl
Innerchr10:12568166..12577793hg19UCSC Ensembl
Innerchr10:12608172..12617799hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg389628
hg199628
hg189628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744012
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549974
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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