A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526194



Internal ID15106801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5413125..5552805hg38UCSC Ensembl
Innerchr7:5452756..5592436hg19UCSC Ensembl
Innerchr7:5419282..5558962hg18UCSC Ensembl
Innerchr7:5225997..5365677hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38139681
hg19139681
hg18139681
hg17139681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702456
Samples
Known GenesACTB, FBXL18, MIR589, TNRC18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526194
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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