A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579879



Internal ID16020602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46119519..46124941hg38UCSC Ensembl
Innerchr19:46622776..46628198hg19UCSC Ensembl
Innerchr19:51314616..51320038hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385423
hg195423
hg185423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6504n54
Supporting Variantsnssv899960, nssv899952, nssv899957, nssv899961, nssv899959, nssv899954, nssv899955, nssv899956, nssv899958, nssv899953
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579879
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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