A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613971



Internal ID16401380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28215696..28355203hg38UCSC Ensembl
Innerchr9:28215694..28355201hg19UCSC Ensembl
Innerchr9:28205694..28345201hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38139508
hg19139508
hg18139508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132115
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613971
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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