A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614057



Internal ID16401466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29218909..30143232hg38UCSC Ensembl
Innerchr9:29218907..30143230hg19UCSC Ensembl
Innerchr9:29208907..30133230hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38924324
hg19924324
hg18924324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156761
Samples1780854339_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614057
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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