A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578231



Internal ID16018954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137305..1148867hg38UCSC Ensembl
Innerchr19:1137304..1148866hg19UCSC Ensembl
Innerchr19:1088304..1099866hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811563
hg1911563
hg1811563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6190n54
Supporting Variantsnssv891683, nssv891684, nssv891678, nssv891681, nssv891682, nssv891680, nssv891679
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578231
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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