A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578954



Internal ID16019677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21404459..21421708hg38UCSC Ensembl
Innerchr19:21587261..21604510hg19UCSC Ensembl
Innerchr19:21379101..21396350hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3817250
hg1917250
hg1817250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6320n54
Supporting Variantsnssv896583
Samples
Known GenesZNF493
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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