A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615262



Internal ID16402671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:117447749..117562075hg38UCSC Ensembl
Innerchr9:120210027..120324353hg19UCSC Ensembl
Innerchr9:119249848..119364174hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38114327
hg19114327
hg18114327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141289
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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