A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3439n100



Internal ID20155055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15166388..15191569hg38UCSC Ensembl
chr19:15277199..15302380hg19UCSC Ensembl
chr19:15138199..15163380hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3825182
hg1925182
hg1825182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061232, nsv1056996, nsv1062099
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)dgv3439n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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