A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578739



Internal ID16019462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17183487..17226535hg38UCSC Ensembl
Innerchr19:17294296..17337344hg19UCSC Ensembl
Innerchr19:17155296..17198344hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3843049
hg1943049
hg1843049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149848
Samples1780854288_A
Known GenesMYO9B, OCEL1, USE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578739
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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