A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899926



Internal ID15847196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44806715..44811138hg38UCSC Ensembl
Innerchr19:45309972..45314395hg19UCSC Ensembl
Innerchr19:50001812..50006235hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384424
hg194424
hg184424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579861
Supporting Variants
Samples
Known GenesBCAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899926
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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