A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608058



Internal ID16048781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102826294..102931266hg38UCSC Ensembl
Innerchr7:102466741..102571713hg19UCSC Ensembl
Innerchr7:102253977..102358949hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38104973
hg19104973
hg18104973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092067
Samples
Known GenesFBXL13, LRRC17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608058
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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