A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615122



Internal ID16055845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105773926..105774791hg38UCSC Ensembl
Innerchr9:108536207..108537072hg19UCSC Ensembl
Innerchr9:107576028..107576893hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38866
hg19866
hg18866
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12839n54
Supporting Variantsnssv1141003, nssv1141004
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615122
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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