A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608059



Internal ID16048782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102830008..102864326hg38UCSC Ensembl
Innerchr7:102470455..102504773hg19UCSC Ensembl
Innerchr7:102257691..102292009hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3834319
hg1934319
hg1834319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092068
Samples
Known GenesFBXL13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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