A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091989



Internal ID15945175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102174515..102183854hg38UCSC Ensembl
Innerchr7:101817795..101827134hg19UCSC Ensembl
Innerchr7:101604515..101613854hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389340
hg199340
hg189340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607995
Supporting Variants
Samples
Known GenesCUX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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