A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613965



Internal ID16401374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28082937..28101543hg38UCSC Ensembl
Innerchr9:28082935..28101541hg19UCSC Ensembl
Innerchr9:28072935..28091541hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3818607
hg1918607
hg1818607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132107
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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