A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045547



Internal ID19134766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18077820..18108318hg38UCSC Ensembl
Innerchr10:18366749..18397247hg19UCSC Ensembl
Innerchr10:18406755..18437253hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3830499
hg1930499
hg1830499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515326
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045547
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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