A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614355



Internal ID16401764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42457827..42458697hg38UCSC Ensembl
Innerchr9:43353497..43354367hg19UCSC Ensembl
Innerchr9:43293493..43294363hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38871
hg19871
hg18871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12704n54
Supporting Variantsnssv1134230, nssv1134231, nssv1134232, nssv1134226, nssv1134228, nssv1134229, nssv1134233, nssv1134227
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614355
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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