A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578255



Internal ID16018978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137713..1138268hg38UCSC Ensembl
Innerchr19:1137712..1138267hg19UCSC Ensembl
Innerchr19:1088712..1089267hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38556
hg19556
hg18556
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891740, nssv891743, nssv891741, nssv891744, nssv891742
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578255
Frequency
Sample Size17421
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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