A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899489



Internal ID16193445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40856268..40875612hg38UCSC Ensembl
Innerchr19:41362173..41381517hg19UCSC Ensembl
Innerchr19:46054013..46073357hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3819345
hg1919345
hg1819345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579578
Supporting Variants
Samples
Known GenesCYP2A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899489
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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