A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578172



Internal ID16018895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:811414..841398hg38UCSC Ensembl
Innerchr19:811414..841398hg19UCSC Ensembl
Innerchr19:762414..792398hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3829985
hg1929985
hg1829985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891240
Samples
Known GenesAZU1, LPPR3, MIR3187, PRTN3, PTBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578172
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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