A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578679



Internal ID16019402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14621900..14622991hg38UCSC Ensembl
Innerchr19:14732712..14733803hg19UCSC Ensembl
Innerchr19:14593712..14594803hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381092
hg191092
hg181092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv894907
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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