A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140997



Internal ID15647497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105705848..105784157hg38UCSC Ensembl
Innerchr9:108468129..108546438hg19UCSC Ensembl
Innerchr9:107507950..107586259hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3878310
hg1978310
hg1878310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615116
Supporting Variants
Samples
Known GenesTMEM38B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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