A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525691



Internal ID15452984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129615309..129619684hg38UCSC Ensembl
Innerchr8:130627555..130631930hg19UCSC Ensembl
Innerchr8:130696737..130701112hg18UCSC Ensembl
Innerchr8:130696737..130701112hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg384376
hg194376
hg184376
hg174376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701850
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525691
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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