A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614147



Internal ID16401556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33434933..33453640hg38UCSC Ensembl
Innerchr9:33434931..33453638hg19UCSC Ensembl
Innerchr9:33424931..33443638hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3818708
hg1918708
hg1818708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176064
Samples1780854215_A
Known GenesAQP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614147
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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