A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522459



Internal ID15103066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144519234..144845293hg38UCSC Ensembl
Innerchr8:145744618..146070678hg19UCSC Ensembl
Innerchr8:145715426..146041482hg18UCSC Ensembl
Innerchr8:145715426..146041482hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38326060
hg19326061
hg18326057
hg17326057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705823
Samples
Known GenesARHGAP39, C8orf82, LRRC14, LRRC24, MIR6850, RPL8, ZNF251, ZNF34, ZNF517, ZNF7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522459
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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