A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578339



Internal ID16019062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1862103..1864258hg38UCSC Ensembl
Innerchr19:1862102..1864257hg19UCSC Ensembl
Innerchr19:1813102..1815257hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382156
hg192156
hg182156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891945
Samples
Known GenesKLF16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578339
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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