A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054644



Internal ID19143863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65401791..65427214hg38UCSC Ensembl
Innerchr10:67161549..67186972hg19UCSC Ensembl
Innerchr10:66831555..66856978hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3825424
hg1925424
hg1825424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522745
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)nsv1054644
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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