A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891638



Internal ID15838908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137305..1138215hg38UCSC Ensembl
Innerchr19:1137304..1138214hg19UCSC Ensembl
Innerchr19:1088304..1089214hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578229
Supporting Variants
Samples
Known GenesSBNO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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