A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615249



Internal ID16402658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114632315..114662575hg38UCSC Ensembl
Innerchr9:117394595..117424855hg19UCSC Ensembl
Innerchr9:116434416..116464676hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3830261
hg1930261
hg1830261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141279
Samples
Known GenesC9orf91
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615249
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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