A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614086



Internal ID16401495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30040354..30154927hg38UCSC Ensembl
Innerchr9:30040352..30154925hg19UCSC Ensembl
Innerchr9:30030352..30144925hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38114574
hg19114574
hg18114574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132490
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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