A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054641



Internal ID19143860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10586341..10658205hg38UCSC Ensembl
Innerchr10:10628304..10700168hg19UCSC Ensembl
Innerchr10:10668310..10740174hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3871865
hg1971865
hg1871865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3496895
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)nsv1054641
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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