A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891838



Internal ID16185794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1567558..1579466hg38UCSC Ensembl
Innerchr19:1567557..1579465hg19UCSC Ensembl
Innerchr19:1518557..1530465hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811909
hg1911909
hg1811909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578312
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)nssv891838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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