A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615266



Internal ID16402675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118089301..118154463hg38UCSC Ensembl
Innerchr9:120851579..120916741hg19UCSC Ensembl
Innerchr9:119891400..119956562hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3865163
hg1965163
hg1865163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141293
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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