A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066831



Internal ID18809362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15173926..15199422hg38UCSC Ensembl
Innerchr19:15284737..15310233hg19UCSC Ensembl
Innerchr19:15145737..15171233hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3825497
hg1925497
hg1825497
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3441n100
Supporting Variantsnssv3564789
Samples
Known GenesMIR6795, NOTCH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066831
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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