A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141280



Internal ID15647780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115005741..115250562hg38UCSC Ensembl
Innerchr9:117768021..118012841hg19UCSC Ensembl
Innerchr9:116807842..117052662hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38244822
hg19244821
hg18244821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615250
Supporting Variants
Samples
Known GenesDEC1, TNC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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