A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891664



Internal ID15838934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137305..1138268hg38UCSC Ensembl
Innerchr19:1137304..1138267hg19UCSC Ensembl
Innerchr19:1088304..1089267hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578230
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)nssv891664
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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