A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614090



Internal ID16054813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30374649..30656886hg38UCSC Ensembl
Innerchr9:30374647..30656884hg19UCSC Ensembl
Innerchr9:30364647..30646884hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38282238
hg19282238
hg18282238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12646n54
Supporting Variantsnssv1132491
Samples
Known GenesLOC401497
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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