A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614879



Internal ID16402288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93121081..93135282hg38UCSC Ensembl
Innerchr9:95883363..95897564hg19UCSC Ensembl
Innerchr9:94923184..94937385hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3814202
hg1914202
hg1814202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139368
Samples
Known GenesNINJ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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