A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615804



Internal ID16403213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134290253..134351537hg38UCSC Ensembl
Innerchr9:137182099..137243383hg19UCSC Ensembl
Innerchr9:136321920..136383204hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3861285
hg1961285
hg1861285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176376
Samples1780862444_A
Known GenesRXRA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615804
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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