A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614097



Internal ID16054820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30420640..30698144hg38UCSC Ensembl
Innerchr9:30420638..30698142hg19UCSC Ensembl
Innerchr9:30410638..30688142hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38277505
hg19277505
hg18277505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12646n54
Supporting Variantsnssv1132505
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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