A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528486



Internal ID15455779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102267694..102361076hg38UCSC Ensembl
Innerchr8:103279922..103373304hg19UCSC Ensembl
Innerchr8:103349098..103442480hg18UCSC Ensembl
Innerchr8:103349098..103442480hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3893383
hg1993383
hg1893383
hg1793383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705090
Samples
Known GenesUBR5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528486
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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