A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528988



Internal ID15456281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89463146..89596017hg38UCSC Ensembl
Innerchr8:90475375..90608246hg19UCSC Ensembl
Innerchr8:90544491..90677362hg18UCSC Ensembl
Innerchr8:90544491..90677362hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38132872
hg19132872
hg18132872
hg17132872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705688
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528988
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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