A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578221



Internal ID16018944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1131175..1148813hg38UCSC Ensembl
Innerchr19:1131174..1148812hg19UCSC Ensembl
Innerchr19:1082174..1099812hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3817639
hg1917639
hg1817639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6185n54
Supporting Variantsnssv891595
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578221
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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