A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578256



Internal ID16018979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137713..1148813hg38UCSC Ensembl
Innerchr19:1137712..1148812hg19UCSC Ensembl
Innerchr19:1088712..1099812hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811101
hg1911101
hg1811101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6195n54
Supporting Variantsnssv891745
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578256
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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