A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054649



Internal ID18797180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44353473..44394265hg38UCSC Ensembl
Innerchr10:44848921..44889713hg19UCSC Ensembl
Innerchr10:44168927..44209719hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3840793
hg1940793
hg1840793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521161
Samples
Known GenesCXCL12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054649
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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