A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578228



Internal ID16018951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137305..1138161hg38UCSC Ensembl
Innerchr19:1137304..1138160hg19UCSC Ensembl
Innerchr19:1088304..1089160hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38857
hg19857
hg18857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6188n54
Supporting Variantsnssv891613, nssv891615, nssv891612, nssv891614
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578228
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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