A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141029



Internal ID15647529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105774587..105775763hg38UCSC Ensembl
Innerchr9:108536868..108538044hg19UCSC Ensembl
Innerchr9:107576689..107577865hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381177
hg191177
hg181177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615138
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)nssv1141029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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