A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578474



Internal ID16365883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6957866..6996498hg38UCSC Ensembl
Innerchr19:6957877..6996509hg19UCSC Ensembl
Innerchr19:6908877..6947509hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3838633
hg1938633
hg1838633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6238n54
Supporting Variantsnssv893198
Samples
Known GenesEMR4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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