A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579606



Internal ID16367015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41553480..41555761hg38UCSC Ensembl
Innerchr19:42059850..42062131hg19UCSC Ensembl
Innerchr19:46751690..46753971hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382282
hg192282
hg182282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6455n54
Supporting Variantsnssv899530, nssv899535, nssv899539, nssv899534, nssv899528, nssv899529, nssv899537, nssv899527, nssv899536, nssv899532, nssv899533, nssv899531, nssv899538
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579606
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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