A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054616



Internal ID18797147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18145025..18163040hg38UCSC Ensembl
Innerchr10:18433954..18451969hg19UCSC Ensembl
Innerchr10:18473960..18491975hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3818016
hg1918016
hg1818016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522721
Samples
Known GenesCACNB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054616
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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