A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578346



Internal ID16019069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1863451..1864961hg38UCSC Ensembl
Innerchr19:1863450..1864960hg19UCSC Ensembl
Innerchr19:1814450..1815960hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381511
hg191511
hg181511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891960
Samples
Known GenesKLF16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578346
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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