A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578167



Internal ID16018890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:797079..850574hg38UCSC Ensembl
Innerchr19:797079..850574hg19UCSC Ensembl
Innerchr19:748079..801574hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3853496
hg1953496
hg1853496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150641
Samples1780862100_A
Known GenesAZU1, LPPR3, MIR3187, MIR4745, PRTN3, PTBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578167
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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