A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614148



Internal ID16401557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33442988..33447555hg38UCSC Ensembl
Innerchr9:33442986..33447553hg19UCSC Ensembl
Innerchr9:33432986..33437553hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384568
hg194568
hg184568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132840
Samples
Known GenesAQP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614148
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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