A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088466



Internal ID15594966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76518274..76519888hg38UCSC Ensembl
Innerchr7:76147591..76149205hg19UCSC Ensembl
Innerchr7:75985527..75987141hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381615
hg191615
hg181615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607620
Supporting Variants
Samples
Known GenesUPK3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1088466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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