A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614824



Internal ID16402233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88739635..88873810hg38UCSC Ensembl
Innerchr9:91354550..91488725hg19UCSC Ensembl
Innerchr9:90544370..90678545hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38134176
hg19134176
hg18134176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139218
Samples
Known GenesMIR4289
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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