A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3419n100



Internal ID20155035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:90898..305459hg38UCSC Ensembl
chr19:90898..305459hg19UCSC Ensembl
chr19:41898..256459hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38214562
hg19214562
hg18214562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058273, nsv1063639, nsv1066301, nsv1066709
Samples
Known GenesLINC01002, OR4F17, PPAP2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3419n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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