A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141353



Internal ID15994539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126614797..126701334hg38UCSC Ensembl
Innerchr9:129377076..129463613hg19UCSC Ensembl
Innerchr9:128416897..128503434hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3886538
hg1986538
hg1886538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615315
Supporting Variants
Samples
Known GenesLMX1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141353
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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