A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv900174



Internal ID15847444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50717680..50760253hg38UCSC Ensembl
Innerchr19:51220937..51263510hg19UCSC Ensembl
Innerchr19:55912749..55955322hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3842574
hg1942574
hg1842574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579951
Supporting Variants
Samples
Known GenesCLEC11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv900174
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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