A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527504



Internal ID15454797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95961915..95973533hg38UCSC Ensembl
Innerchr7:95591227..95602845hg19UCSC Ensembl
Innerchr7:95429163..95440781hg18UCSC Ensembl
Innerchr7:95235878..95247496hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811619
hg1911619
hg1811619
hg1711619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703956
Samples
Known GenesDYNC1I1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527504
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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