A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579277



Internal ID16366686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29566638..29567736hg38UCSC Ensembl
Innerchr19:30057545..30058643hg19UCSC Ensembl
Innerchr19:34749385..34750483hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6394n54
Supporting Variantsnssv897580
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579277
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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