A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528821



Internal ID15456114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:108003570..108008172hg38UCSC Ensembl
Innerchr8:109015798..109020400hg19UCSC Ensembl
Innerchr8:109084974..109089576hg18UCSC Ensembl
Innerchr8:109084974..109089576hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg384603
hg194603
hg184603
hg174603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705495
Samples
Known GenesRSPO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528821
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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