A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615117



Internal ID16055840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105772224..105774530hg38UCSC Ensembl
Innerchr9:108534505..108536811hg19UCSC Ensembl
Innerchr9:107574326..107576632hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382307
hg192307
hg182307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140998
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615117
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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