A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613670



Internal ID16401079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16484733..16516943hg38UCSC Ensembl
Innerchr9:16484731..16516941hg19UCSC Ensembl
Innerchr9:16474731..16506941hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3832211
hg1932211
hg1832211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156253
Samples1780854128_A
Known GenesBNC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613670
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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