A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901189



Internal ID15848459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53977896..53989668hg38UCSC Ensembl
Innerchr19:54481150..54492922hg19UCSC Ensembl
Innerchr19:59172962..59184734hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3811773
hg1911773
hg1811773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580111
Supporting Variants
Samples
Known GenesCACNG8, MIR935
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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