A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522308



Internal ID15449601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136134175..136273945hg38UCSC Ensembl
Innerchr8:137146418..137286188hg19UCSC Ensembl
Innerchr8:137215600..137355370hg18UCSC Ensembl
Innerchr8:137215600..137355370hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38139771
hg19139771
hg18139771
hg17139771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695088
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522308
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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