A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066301



Internal ID18808832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:90898..277776hg38UCSC Ensembl
Innerchr19:90898..277776hg19UCSC Ensembl
Innerchr19:41898..228776hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38186879
hg19186879
hg18186879
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3419n100
Supporting Variantsnssv3563114
Samples
Known GenesLINC01002, OR4F17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066301
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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