A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526062



Internal ID15453355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104177149..104250637hg38UCSC Ensembl
Innerchr7:103817597..103891085hg19UCSC Ensembl
Innerchr7:103604833..103678321hg18UCSC Ensembl
Innerchr7:103411548..103485036hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3873489
hg1973489
hg1873489
hg1773489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702301
Samples
Known GenesORC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526062
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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