A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525292



Internal ID15105899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91110980..91161887hg38UCSC Ensembl
Innerchr8:92123208..92174115hg19UCSC Ensembl
Innerchr8:92192384..92243291hg18UCSC Ensembl
Innerchr8:92192384..92243291hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3850908
hg1950908
hg1850908
hg1750908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701398
Samples
Known GenesLRRC69
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525292
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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