A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891719



Internal ID15838989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1137402..1152657hg38UCSC Ensembl
Innerchr19:1137401..1152656hg19UCSC Ensembl
Innerchr19:1088401..1103656hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3815256
hg1915256
hg1815256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578240
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)nssv891719
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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