A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615774



Internal ID16403183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134005665..134073839hg38UCSC Ensembl
Innerchr9:136870787..136938961hg19UCSC Ensembl
Innerchr9:135860608..135928782hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3868175
hg1968175
hg1868175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176372
Samples1780862416_A
Known GenesBRD3, LINC00094
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615774
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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