A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891808



Internal ID15839078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566455..1566989hg38UCSC Ensembl
Innerchr19:1566454..1566988hg19UCSC Ensembl
Innerchr19:1517454..1517988hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38535
hg19535
hg18535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578298
Supporting Variants
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891808
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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