A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578259



Internal ID16018982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137824..1148658hg38UCSC Ensembl
Innerchr19:1137823..1148657hg19UCSC Ensembl
Innerchr19:1088823..1099657hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810835
hg1910835
hg1810835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6195n54
Supporting Variantsnssv891757
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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