A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899993



Internal ID16193949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49930731..49969159hg38UCSC Ensembl
Innerchr19:50433988..50472416hg19UCSC Ensembl
Innerchr19:55125800..55164228hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3838429
hg1938429
hg1838429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579911
Supporting Variants
Samples
Known GenesATF5, MIR4751, SIGLEC11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899993
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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