A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615287



Internal ID16056010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123994361..124052300hg38UCSC Ensembl
Innerchr9:126756640..126814579hg19UCSC Ensembl
Innerchr9:125796461..125854400hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3857940
hg1957940
hg1857940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141315
Samples
Known GenesLHX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615287
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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