A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579570



Internal ID16366979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40850846..40873243hg38UCSC Ensembl
Innerchr19:41356751..41379148hg19UCSC Ensembl
Innerchr19:46048591..46070988hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3822398
hg1922398
hg1822398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6446n54
Supporting Variantsnssv899477, nssv899472, nssv899473, nssv899475, nssv899474, nssv899476
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579570
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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