A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141351



Internal ID15647851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126578413..126646919hg38UCSC Ensembl
Innerchr9:129340692..129409198hg19UCSC Ensembl
Innerchr9:128380513..128449019hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3868507
hg1968507
hg1868507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615313
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)nssv1141351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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