A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062099



Internal ID18804630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15171818..15191569hg38UCSC Ensembl
Innerchr19:15282629..15302380hg19UCSC Ensembl
Innerchr19:15143629..15163380hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3819752
hg1919752
hg1819752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3439n100
Supporting Variantsnssv3564787
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)nsv1062099
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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