A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578345



Internal ID16019068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1863451..1864602hg38UCSC Ensembl
Innerchr19:1863450..1864601hg19UCSC Ensembl
Innerchr19:1814450..1815601hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381152
hg191152
hg181152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891959
Samples
Known GenesKLF16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578345
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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