A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578294



Internal ID16019017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1467771..1472331hg38UCSC Ensembl
Innerchr19:1467770..1472330hg19UCSC Ensembl
Innerchr19:1418770..1423330hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384561
hg194561
hg184561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891805
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578294
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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