A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613749



Internal ID16401158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20817349..20897267hg38UCSC Ensembl
Innerchr9:20817348..20897266hg19UCSC Ensembl
Innerchr9:20807348..20887266hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3879919
hg1979919
hg1879919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156452
SamplesNINDS_145
Known GenesFOCAD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613749
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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