A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578667



Internal ID16019390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14621589..14622371hg38UCSC Ensembl
Innerchr19:14732401..14733183hg19UCSC Ensembl
Innerchr19:14593401..14594183hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38783
hg19783
hg18783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv894853
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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