A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615961



Internal ID16056684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136124480..136233010hg38UCSC Ensembl
Innerchr9:139016326..139124856hg19UCSC Ensembl
Innerchr9:138156147..138264677hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38108531
hg19108531
hg18108531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13001n54
Supporting Variantsnssv1148321
Samples
Known GenesLHX3, QSOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615961
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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