A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891822



Internal ID15839092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566455..1577238hg38UCSC Ensembl
Innerchr19:1566454..1577237hg19UCSC Ensembl
Innerchr19:1517454..1528237hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810784
hg1910784
hg1810784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578302
Supporting Variants
Samples
Known GenesMBD3, MEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891822
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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