A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615316



Internal ID16402725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126660504..126700316hg38UCSC Ensembl
Innerchr9:129422783..129462595hg19UCSC Ensembl
Innerchr9:128462604..128502416hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3839813
hg1939813
hg1839813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176495
Samples1780854418_A
Known GenesLMX1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615316
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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