A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061882



Internal ID19151101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10704200..10737778hg38UCSC Ensembl
Innerchr19:10814876..10848454hg19UCSC Ensembl
Innerchr19:10675876..10709454hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3833579
hg1933579
hg1833579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564688
Samples
Known GenesDNM2, MIR638, QTRT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061882
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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