A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578280



Internal ID16019003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1457898..1470022hg38UCSC Ensembl
Innerchr19:1457897..1470021hg19UCSC Ensembl
Innerchr19:1408897..1421021hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812125
hg1912125
hg1812125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891785
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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