A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899990



Internal ID15847260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49022757..49044395hg38UCSC Ensembl
Innerchr19:49526014..49547652hg19UCSC Ensembl
Innerchr19:54217826..54239464hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3821639
hg1921639
hg1821639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579907
Supporting Variants
Samples
Known GenesCGB, CGB1, CGB2, CGB5, SNAR-G1, SNAR-G2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899990
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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