A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578232



Internal ID16018955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137305..1152657hg38UCSC Ensembl
Innerchr19:1137304..1152656hg19UCSC Ensembl
Innerchr19:1088304..1103656hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3815353
hg1915353
hg1815353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6187n54
Supporting Variantsnssv891686, nssv891685, nssv891687
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578232
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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