A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051284



Internal ID19140503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16279533..16350127hg38UCSC Ensembl
Innerchr10:16321532..16392126hg19UCSC Ensembl
Innerchr10:16361538..16432132hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870595
hg1970595
hg1870595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513714
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)nsv1051284
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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